Sunday, July 30, 2017

Salmonella Outbreak Exposes Flaw in FDA ‘Import Alert’ System

The Food and Drug Administration (FDA), the Centers for Disease Control and Prevention (CDC), the Maryland Department of Health (MDH) and other state and local agencies continue to investigate the  outbreak of Salmonella Kiambu illnesses, which has sickened 47 people and has already claimed one life.

The CDC posted this photo with the outbreak notice, describing maradol papayas as large, oval fruits that weigh 3 or more pounds, with green skins that turn yellow when the fruit is ripe. The flesh inside the fruit is salmon-colored.” Photo courtesy of CDC

Based on sampling and analysis reported by MDH, the outbreak appears to be linked to consumption of Maradol papayas, imported from Mexico. On July 26, 2017, Grande Produce (San Juan, TX) recalled Caribeña brand Maradol papayas that were shipped to an unnamed Maryland distributor center between July 10 and July 19.

The introduction of Salmonella-contaminated papayas into the US retail market occurred despite the issuance in August 2011 of Import Alert 21-17, COUNTRYWIDE DETENTION WITHOUT PHYSICAL EXAMINATION OF PAPAYA FROM MEXICO.

What is an Import Alert?

An Import Alert informs “…FDA field staff and the public that the agency has enough evidence to allow for Detention Without Physical Examination (DWPE) of products that appear to be in violation of FDA laws and regulations.” It can be very narrow (apply to a single company or importer) or extremely broad, as in the case of Import Alert 21-17. The purpose of the Import Alert is to place the burden of proving product safety on the shoulders of the producer or importer. The first Import Alert was issued in 1974.

History of Import Alert 21-17

Mexican papayas were the source of a Salmonella Agona outbreak that sickened 106 people in 25 US states between January 1 and August 25, 2011. The outbreak was traced to several brands of papayas distributed in the USA and Canada by Agromod Produce, Inc.

During the investigation into the source of the outbreak, FDA analyzed 211 samples of Mexican papayas, finding Salmonella in 33 (15.6 percent) of them. The positive samples came from 28 different firms and nearly all the major papaya-growing regions of Mexico. In response to the extent of the contamination, FDA issued Import Alert 21-17 on August 25, 2011.

Are there any exceptions to the Import Alert?

FDA policy allows for exemptions to an Import Alert, if a company can provide evidence that their products are likely to remain in compliance with FDA laws and regulations. In the case of Import Alert 21-17, FDA considers Salmonella-negative test results from five consecutive shipments over a period of time to be evidence of probable compliance. Entities able to meet these criteria may apply for an exemption. If accepted, they are added to  the Green List appended to the Import Alert.

How does the Green List Work?

At last count, FDA has granted 98 exemptions in the nearly six years during which the Import Alert has been in force. Once granted, exemptions remain in effect unless FDA receives evidence of lack of compliance, such as a result of a consumer complaint, a Salmonella-positive routine retail surveillance sample. There is no requirement for inspection of the exempt entity’s operations, for routine or periodic submission of lab test results, or for any other form or recertification. A Green-listed entity under Import Alert 21-17 has carte-blanche to ship papayas from Mexico into the USA.

What Happens to Detained Shipments under Import Alert 21-17?

Entities whose products are detained without physical examination may apply to have those products released by submitting evidence from a third-party laboratory that the product is not contaminated with Salmonella. Otherwise, the product either will be refused entry into the USA, or will be destroyed.

The action taken last week by Grande Produce represents the second time in recent years that Caribeña brand Mexican papayas have been recalled due to Salmonella contamination. The first recall took place in May 2012 after routine testing by Caribe Produce, LTD CO discovered Salmonella contamination.

A recent search of Texas Secretary of State corporate filings revealed Raul Cano to be both the registered agent for Caribe Produce and a Managing Member/Director of Grande Produce. Both companies currently share the same street address. According to a May 2017 article published in Texas Border Business, Grande Produce is owned jointly by Raul Cano and his brother, Juan Cano.

While the identity of the Mexican grower who supplied the recalled papayas has not been determined, Chiapas-based Finca Monte Verde identifies its US distributor to be Grande Produce and identifies Caribe Produce as its contact point in the USA. Finca Monte Verde is on the Import Alert 21-17 Green List and, therefore, is exempt from automatic detention.

There is no information on either the Finca Monte Verde or the Grande Produce websites to indicate whether or not Finca Monte Verde is the sole supplier of papayas to Grande Produce. While FDA is conducting a traceback investigation of the recalled Caribeña papayas, its investigators also are working with CDC and state agencies to determine whether other brands of papayas may be implicated in the Salmonella outbreak.

Although the investigating state and federal agencies have not yet determined the origin of the contaminated papayas, or the point in the tree-to-table distribution chain at which they may have become contaminated, one thing is certain. Either the papayas entered the USA under the aegis of a Green-Listed entity or the produce was admitted as a result of a third-party lab analysis certifying a Salmonella-negative result.

As food safety advocate Bill Marler pointed out in his recent opinion piece, ‘Why the US imports tainted food that can kill you,’ FDA’s ability to carry out proactive inspections of foreign growers and packers is severely limited by budget constraints, forcing the agency to rely on the good faith and probity of these entities and of their third-party testing laboratories to deliver a safe product to US consumers.

In this case, it seems the outcome was a large gap in the food safety border wall—maybe large  enough to drive a refrigerated 18-wheeler through.

 

Editor’s Note: Attorney Bill Marler is the publisher of Food Safety News.

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Thursday, July 27, 2017

More distributors, brands likely involved in papaya outbreak

Editor’s note: Because of the popularity of papayas in Mexican and Hispanic cuisine, public health officials say people in those groups are at particular risk during the current outbreak. To access information the CDC has posted in Spanish, click here. 

Federal officials doubled down on warnings about whole, fresh maradol papayas Thursday, urging consumers to throw out the tropical fruit — especially if they are not sure of its brand or country of origin — because it is linked to an ongoing Salmonella outbreak that has killed one and sickened 46 others.

Maradol papayas are a large, oval fruit that weighs 3 or more pounds, with green skins that turn yellow when the fruit is ripe. The flesh inside the fruit is salmon-colored. Photo courtesy of CDC

There is a good chance consumers still have Caribeña brand maradol papayas in their homes and the fruit could still be in the supply chain, even though one distributor has initiated a recall, federal agencies reported.

Grande Produce LLC of San Juan, TX, has recalled Caribeña brand maradol papayas that it distributed nationwide from July 10-19 because Maryland officials found them to be contaminated with the same strain of Salmonella Kiambu that has infected outbreak victims.

However, federal officials say other distributors and/or other brands are likely also involved.

“The FDA is warning consumers to avoid all Caribeña brand maradol papayas,” the agency said Thursday in an outbreak investigation update, but also noted that “there are illnesses in states where Grande Produce did not distribute papayas…

“FDA continues its traceback investigation. … Additional brands will be announced as the information becomes available.”

While FDA has not specified a country of origin for the implicated fruit, maradol papayas from Mexico are specifically named in advice from the Centers for Disease Control and Prevention.

“CDC recommends that consumers not eat, restaurants not serve, and retailers not sell maradol papayas from Mexico until we learn more,” according to the Thursday outbreak update.

“Additional brands will be announced as the information becomes available. If you aren’t sure if the papaya you bought is a Maradol papaya from Mexico, you can ask the place of purchase. Restaurants and retailers can ask their supplier.

“When in doubt, don’t eat, sell, or serve them and throw them out. Wash and sanitize countertops as well as drawers or shelves in refrigerators where papayas were stored.”

The CDC’s Thursday update showed the number of confirmed Salmonella Kiambu infection cases holding steady at 47, as of July 21. Of 33 people who have been interviewed, a dozen had symptoms so severe they required hospitalization. A list of the states with confirmed cases and the number of sick people in each is available on CDC’s Case Count Map page. Confirmed illnesses started on dates ranging from May 17 to June 28.

An FDA spokesman said Thursday the agency is concerned that some consumers may
have misunderstood initial warnings that referenced “yellow maradol papayas.” He said the color has been removed from warnings and outbreak updates because the fruit is often shipped and sold while it is still green.

“Maradol papayas are green before they ripen and turn yellow, so consumers should not eat Caribeña brand regardless of the color,” according to the most recent FDA outbreak update.

“If anyone has these papayas in their home, they should dispose of them immediately. These can be identified by a red, green and yellow sticker shown (at right).”

Symptoms of infection
Anyone who has eaten fresh papaya recently and developed symptoms of Salmonella infection is urged to seek medical attention and tell their doctors about the possible exposure so the proper diagnostic tests can be performed.

Salmonella bacteria can cause diarrhea, vomiting, stomach pain and fever. Symptoms usually begin between 12 to 36 hours after exposure, but they may begin as early as 6 hours or as late as 72 hours after exposure.

Symptoms can be mild or severe and commonly last for two to seven days. Salmonella can infect anyone, but young children, older adults and people with weakened immune systems are the most likely to have severe infections.

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EU adopts measures to reduce levels of acrylamide in food

Representatives from the European Union (EU) Member States have voted in favor of the European Commission’s (EC) proposal to reduce the presence of acrylamide in food.

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FDA approves qualified health claim for macadamia nuts

After conducting a systematic review of the available scientific data, the U.S. Food and Drug Administration (FDA) now intends to exercise enforcement discretion over the use of a qualified health claim characterizing the relationship between consumption of macadamia nuts and reduced risk of coronary heart disease.

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Judge dismisses ‘natural’ suit against General Mills

According to the Star Tribune, a federal judge has dismissed a class-action lawsuit against General Mills over the company’s use of “natural” to describe the oats in its Nature Valley granola bars.

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PepsiCo promotes Laguarta to president

PepsiCo has announced three senior leadership appointments that support the company’s strategic priorities and growth agenda.

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U.S., China sign agreement to provide market access for U.S. rice exports

U.S. Secretary of Agriculture Sonny Perdue has announced that the U.S. Dept. of Agriculture (USDA) has reached agreement with Chinese officials on final details of a protocol to allow the United States to begin exporting rice to China for the first time ever.

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Germany is No. 2 in ‘superfood’ launches

New research from global market intelligence agency Mintel shows that Germany has recently overtaken Australia and the United Kingdom, and is now the second most innovative market for “superfood” launches.

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Grupo Bimbo to acquire East Balt Bakeries for $650 million

Grupo Bimbo has announced an agreement to acquire East Balt Bakeries, a global leader within the foodservice industry, for $650 million.

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NASA teams up with Tupperware, Techshot to improve plant growth in space

The National Aeronautics and Space Administration (NASA), Techshot, and Tupperware Brands have partnered to develop an improved system for growing plants aboard the International Space Station (ISS).

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USDA engineers develop sensor system to improve peanut drying

A sensor network developed by U.S. Dept. of Agriculture (USDA) Agricultural Research Service (ARS) engineers could make it easier and cheaper for peanut growers and processors to dry their peanuts.

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Anheuser-Busch acquires Hiball

Anheuser-Busch (A-B) has announced its acquisition of Hiball, maker of organic energy drinks and sparkling energy waters, as well as Alta Palla (“high ball” in Italian), a brand of organic sparkling juices and sparkling waters.

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Campbell creates position to lead digital, e-commerce

Campbell Soup has announced the appointment of Shakeel Farooque to the newly created role of vice president and head of digital and e-commerce.

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FDA: Papayas linked to multiple Salmonella outbreak strains

The U.S. Food and Drug Administration (FDA), along with the Centers for Disease Control and Prevention (CDC), the Maryland Dept. of Health (MDH), and other state and local partners, is investigating multiple Salmonella illnesses, some of which are linked to Caribeña brand Maradol papayas from Mexico and distributed by Grande Produce in San Juan, Texas.

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Schwan’s expands pizza capabilities with two acquisitions

Schwan’s has acquired from NE Foods Inc. its wholly owned subsidiaries of Better Baked Foods and Drayton Foods.

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FAO issues alert over continued drought, worsening hunger in East Africa

Poor rains across East Africa have worsened hunger and left crops scorched, pastures dry, and thousands of livestock dead, according to an alert released by the United Nations’ Food and Agriculture Organization (FAO).

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More than 100 million Americans have diabetes or prediabetes

The U.S. Centers for Disease Control & Prevention (CDC) has released “The National Diabetes Statistics Report,” which finds that an estimated 30.3 million people of all ages—or 9.4% of the U.S. population—had diabetes in 2015.

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Report: Food waste reduction, reuse

The report—“Food Waste Erased”—gives an overview of various public- and private-sector initiatives for reducing food waste at various levels, from individual best practices to international policy.

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Safer meat requires reducing risks where food animals are raised

Wider use of evidence-based food safety interventions on farms and feedlots would significantly reduce the risk of people getting sick from contaminated meat and poultry, according to a report by The Pew Charitable Trusts.

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Wednesday, July 26, 2017

Importer finally recalls papayas linked to deadly outbreak

A week after Maryland officials issued a public warning linking Caribeña  brand maradol papayas to a Salmonella outbreak, produce distributor Grande Produce LLC finally went public with a recall of the implicated fruit.

In the company’s recall notice, posted late Wednesday by the Food and Drug Administration, Grande Produce of San Juan, TX, reported it has stopped receiving papayas from the grower in Mexico that supplied the fruit linked to the outbreak. Neither the grower nor the region of Mexico where the papayas came from have been identified.

As of Tuesday, one person had died and 46 others across a dozen states had been lab-confirmed with infections from the outbreak strain of Salmonella, according to the Centers for Disease Control and Prevention. Twelve of the victims had symptoms so severe they required hospitalization.

Maryland officials collected papayas from a grocery store in Baltimore where some sick people said they shopped. Laboratory tests showed the fruit was contaminated with the same strain of Salmonella isolated from the sick people.

“Environmental microbial testing conducted by Grande Produce of its facilities has been negative for the Salmonella organism to date” according to the recall notice on the FDA website.

“The company is coordinating closely with the U.S. Food and Drug Administration and other regulatory agencies in their investigations and will provide any assistance possible.”

Grande Produce did not provide distribution details about regions or specific retailers that received the recalled Caribeña brand maradol papayas. Its recall notice did confirm that it distributed papayas in Maryland, where at least five people have been confirmed as outbreak victims.

The recalled papayas distributed by Grande Produce may have these stickers on them.

“(The) Maryland distribution center where the papayas were delivered has already notified retail customers to remove the recalled papayas from inventories, store shelves and the stream of commerce,” according to the Wednesday recall notice.

Distribution dates for the papayas recalled by Grande Produce run from July 10 through July 19, according to the Wednesday recall notice.

However, in its Tuesday consumer alert, FDA reported different distribution dates and reported that the company had not gone public with the recall. The agency

“Grande Produce has informed the FDA that the company initiated a limited recall of their Caribeña brand Maradol papayas distributed nationwide from July 7 – July 18,” FDA reported Tuesday.

“As of July 25, Grande Produce has not issued a press release to notify consumers of their recall. Therefore, FDA is advising consumers to avoid all Caribeña brand Maradol papayas. The FDA also noted that there are illnesses in states where Grande Produce did not distribute papayas and is continuing its investigation.”

As of Wednesday night, Food Safety News had not received any responses to requests for comment sent to Grande Produce officials CEO Juan Cano, COO Raul Cano, and Food Safety Advisor Abraham Dajlala.

Earlier Wednesday, grocery retailer Aldi posted a recall notice on its website for all brands maradol papayas, citing federal and state warnings about the Salmonella outbreak.

Walmart posted a link to the CDC’s outbreak alert on the recall page of its website.

As of Wednesday night, Grande Produce had not posted any recall information on its website. The company was still offering maradol papayas of undeclared origin for sale.

“Consumers who may have purchased the Caribeña brand of papayas are advised not to eat them and to dispose of them instead. A full refund is available where purchased or from Grande Produce at 888-507-2720,” according to the recall notice on the FDA website.

Advice to consumers, restaurants and retailers
State and federal public health officials recommend applying the golden rule of food safety regarding papayas on hand in homes and businesses: When in doubt, throw it out.

Additional recommendations from CDC include:

  • If you aren’t sure if the papaya you bought is a yellow Maradol papaya, you can ask the place of purchase. Restaurants and retailers can ask their suppliers.
  • If you have had whole, fresh papayas in your home or business, wash and sanitize countertops, cutting boards and utensils, as well as drawers or shelves in refrigerators where papayas were stored, with a solution of one tablespoon of chlorine bleach to one gallon of hot water; dry with a clean cloth or new paper towel.
  • Wash your hands with running water and soap following the cleaning and sanitation process.

Anyone who has eaten fresh papaya recently and developed symptoms of Salmonella infection is urged to seek medical attention and tell their doctors about the possible exposure so the proper diagnostic tests can be performed.

Salmonella bacteria can cause diarrhea, vomiting, stomach pain and fever. Symptoms usually begin between 12 to 36 hours after exposure, but they may begin as early as 6 hours or as late as 72 hours after exposure.

Symptoms can be mild or severe and commonly last for two to seven days. Salmonella can infect anyone, but young children, older adults and people with weakened immune systems are the most likely to have severe infections.

In the current outbreak, illnesses began on May 17, with the most recent confirmed case having reported symptom onset on June 28. The CDC believes additional victims will be identified because of the lag time between illness onset and when local health officials report the cases to state and federal authorities. People who became sick after June 23 could easily not yet be included in the victim count.

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Tuesday, July 25, 2017

D&D Foods recalls almost 9 tons of pizzas made for Hy-Vee brand

Omaha’s D & D Foods Inc. has recalled 17,847 pounds of pepperoni pizza products because of misbranding and an undeclared allergen, according to the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS).

The products contain soy lecithin, a known allergen which is not declared on the product labels. It is a Class II recall with relatively low risk to human health, according to the recall notice.

The pepperoni pizza items were produced and packaged on various dates from April 18, 2017 to July 21.  Subject to the recall are:

  • Cases containing four 32-oz., individually packaged pizzas of “Hy-Vee PEPPERONI PIZZA 16″ THIN CRUST” with case code of 88943.
  • Cases containing four 27-oz., individually packaged pizzas of “Hy-Vee PEPPERONI PIZZA 12″ TRADITIONAL CRUST” with case code 88901.
  • Cases containing four 47-oz., individually packaged pizzas of “Hy-Vee PEPPERONI PIZZA 16″ TRADITIONAL CRUST” with case code 88929.
  • Cases containing four 19-oz., individually packaged pizzas of “Hy-Vee PEPPERONI PIZZA 12″ THIN CRUST” with case code 88915.

The products subject to recall bear establishment number “EST. M21275” inside the USDA mark of inspection on the label. These items were shipped to retail locations in Minneapolis.

The problem was discovered on July 22 by FSIS’ Inspection Program Personnel while performing routine label verification activities.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.

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Distributor recalled papaya for Salmonella; didn’t tell public

Grande Produce LLC, the importer of Caribeña brand Maradol papayas linked to a deadly and ongoing Salmonella outbreak, has “initiated a limited recall” of the fruit distributed nationwide from July 10-19, according to the Food and Drug Administration — but the company has not made the recall public.

Because the company, based in San Juan, TX, has not revealed the recall to the public, the federal agency is warning consumers to avoid all Caribeña brand Maradol papayas because they have been linked to a Salmonella outbreak that has killed one person and sickened 46 others across 12 states.

FDA and the Centers for Disease Control and Prevention, the Maryland Department of Health and other state and local public health agencies are investigating the outbreak.

FDA is advising consumers to avoid all Caribeña brand Maradol papayas. The FDA also noted that there are illnesses in states where Grande Produce did not distribute papayas and is continuing its investigation.

The CDC posted this photo with its outbreak notice. Photo courtesy of CDC

According to FDA’s update, posted this afternoon:

  • Consumers should not to eat Caribeña brand Maradol papayas because they are linked to an outbreak of salmonellosis. Maradol papayas are green before they ripen and turn yellow, so consumers should not eat Caribeña brand regardless of the color. If anyone has these papayas in their home, they should dispose of them immediately. These can be identified by a red, green and yellow sticker.
  • Papaya samples taken by MDH from a Baltimore retail location tested positive for the strains of Salmonella Kiambu and Thompson found in ill people.
  • CDC recommends people should not eat Maradol papayas from Mexico. FDA continues its traceback investigation. At this time, Caribeña brand papayas from Mexico have been identified as a brand linked to these illnesses. Additional brands will be announced as the information becomes available.
  • CDC reports 47 cases,12 hospitalizations and one death from 12 states in the Salmonella Kiambu outbreak. The states involved are IA, KY, LA, MA, MD, MN, NJ, NY, PA, TX, UT and VA. CDC is working to collect additional information to determine whether the recent Salmonella Thompson illness in Maryland is part of this multistate outbreak.

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Monday, July 24, 2017

Stefano’s Foods recalls 981 pounds of Stromboli products

The Charlotte, NC-based Stefano’s Foods Inc. has recalled 981 pounds of Stromboli products because of misbranding and an undeclared allergen, according to  the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS). The product contains eggs, a known allergen which is not declared on the product label.

The frozen meatball Stromboli items, produced on June 24, were incorrectly packaged in boxes labeled as pepperoni and Italian sausage Stromboli.  Recalled are:

  • 18.5-oz. boxes containing two pieces of “SCREAMIN’ SICILIAN PIZZA CO. STROMBOLI SUPREMUS MAXIMUS PEPPERONI & ITALIAN SAUSAGE” with an “Enjoy by: 2/19/2018” date and lot code of 70010117517.

The products subject to recall bear establishment number “EST. 19140” inside the USDA mark of inspection. These items were shipped to a distribution center in Wisconsin.

The mistake was discovered on July 21 by a company employee during the firm’s routine product packaging activities.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website .

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Sunday, July 23, 2017

Bush’s Best recalls beans because can seams are compromised

Bush Brothers & Co. is recalling three flavors of canned baked beans from retailers nationwide after discovering defective side seams in some cans, which could allow the beans to spoil or become contaminated with pathogens.

To view photos of all three flavors of Bush’s Beans subject to this recall, please click on the image.

“This recall was initiated after our internal quality assurance checks identified the issue. Subsequent investigations indicated a temporary quality issue from one of our can suppliers. The problem was corrected and no other product is affected,” according to the July 22 recall notice the company posted on its website.

“It’s important to note that, to date, no illnesses or other adverse consequences have been reported in connection with this voluntary recall; however, we urge you to dispose of these affected products immediately even if the beans do not look or smell spoiled. We are working with our retailers to ensure timely removal of affected product from their warehouses and shelves.”

Three flavors of Bush’s canned baked beans are included in the recall. All beans subject to the recall are in 28-ounce cans. Consumers, retailers and others should check any beans they have on hand to see if they are included in the recall.

See the chart below for the specific information to look for on the cans that will identify the recalled beans.

The company’s consumer relations department is available to answer questions at 800-590-3797, Monday-Friday between 8 a.m. and 5 p.m. Eastern time.

Bush’e Best

Case UPC

Case Lot #

Container UPC

Container Lot #

28 OZ
BROWN SUGAR HICKORY

003940001977   

001977
12-28 OZ 6097V
BEST BY
JUNE 2019

00039400019770   

6097S GF
6097P GF
BEST BY JUN 2019

28 OZ
COUNTRY
STYLE

003940091974
or
003940001974

001974
12-28 OZ 6077V
AND 6087V
BEST BY
JUNE 2019

00039400019749

6077S RR 6087S RR 6077P RR 6087P RR

BEST BY JUN 2019

28 OZ
ORIGINAL

003940091614
or
003940001614

001614
12-28 OZ 6077V
BEST BY
JUNE 2019

00039400016144

6057S LC
6057P LC
BEST BY JUN 2019

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Friday, July 21, 2017

Idaho Foodbank recalls 13.5 tons of food because of cooler issue

The Idaho Foodbank is recalling 13.5 tons of soup, eggs, cheese and coconut beverages after discovering a refrigeration malfunction, which could have allowed the growth of bacteria and life-threatening pathogens.

To view the full-sized photographs of food recalled by the Idaho Foodbank, please click on the image.

“The Idaho Foodbank discovered the problem after reviewing cooler temperature records during high heat,” according to the recall notice posted on the Food and Drug Administration’s website Friday evening.

The implicated foods and beverages were distributed July 10 through 14 from two regional food bank locations — one in Southwest Idaho and the other in North-Central Idaho — to schools, mobile pantries, community meal sites, school pantries and senior centers.

Brand names of the recalled products were not included in the recall notice, but photos were provided of the coconut beverage, broccoli cheddar soup, eggs and cheese.

“Consumers who obtained any of these identified products should not consume these products and immediately throw them away. No reported illnesses or injuries have been reported or confirmed to date,” according to the recall notice.

“This recall affects less than 2 percent of the 1.5 million pounds of food IFB distributes statewide each month. Consumers with questions or concerns about this recall can contact Jennifer Erickson by phone at 208-336-9643 or via email at jerickson@idahofoodbank.org.

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Bhu Foods recalls protein bars because of Listeria risk

Another brand of protein snacks, Bhu Foods of San Diego, is under recall because they contain organic sunflower seeds from Hudson Valley Foods Inc., which reported finding Listeria monocytogenes in its production facility in recent weeks.

“As a result of a recall of sunflower seeds from Hudson Valley Foods Inc., Bhu Foods’ supplier of organic sunflower seeds, advised Bhu Foods that ingredients sold to the company have the potential to be contaminated with Listeria monocytogenes,” according to the recall notice posted Friday evening by the Food and Drug Administration.

“All affected distributors and retail website customers have been notified and the affected products have been removed from store shelves and inventories. The product was available nationwide in retail stores as well as by mail order/direct delivery.”

No confirmed illnesses had been reported in connection with the Bhu Foods protein bars as of the posting of the recall notice.

The recalled Bhu Foods protein bars were produced from May 9 through June 9 this year. Consumers can identify the recalled bars by looking for the following information on the wrappers, the lot code is printed next to the expiration date:

  • Organic Vegan Protein – Chocolate + Tart Cherry + Pistachio with Lot Code 13717;
  • Organic Vegan Protein – Apple Chunk + Cinnamon + Nutmeg with Lot Code 13717;
  • Organic Vegan Protein – Peanut Butter + Chocolate Chip with Lot Code 13917;
  • Organic Vegan Protein – Superfood Chocolate Chip + Fudge Brownie Batter with Lot Code 13817 or 15417;
  • Organic Vegan Protein – Peanut Butter + White Chocolate with Lot Code 15317 or 15417;
  • Grass Fed Whey Protein – Dark Chocolate + Coconut + Almond “Made with Organic Ingredients” with Lot Code 13917;
  • Grass Fed Whey Protein – Salted Caramel + Pecan “Made with Organic Ingredients” with Lot Code 13017 or 13817;
  • Grass Fed Whey Protein – Vanilla + Almond + Cashew “Made with Organic Ingredients” with Lot Code 13017 or 13817; and
  • Paleo Protein – Double Dark Chocolate Chip “Made with Organic Ingredients” with Lot Code 13117, 14017 or 14317.

“The potential for contamination was noted after routine testing by Hudson Valley Farms. Bhu Foods was notified directly by Hudson Valley Farms and the FDA of the potential contamination and risk for illness from this product. Bhu Foods immediately ceased production and distribution upon receiving this news for the consideration of our consumers,” according to the recall notice.

Consumers should not consume these products. Affected product may be returned to the place of purchase for an exchange. Consumers with questions may contact Bhu Foods at 619-855-3992.

Anyone who has eaten any of the recalled products and developed symptoms of Listeria infection should seek medical attention and tell their doctors about the possible exposure. Additionally, anyone who has eaten the above products recently should monitor themselves for symptoms during the coming weeks because it can take up to nine weeks after exposure for symptoms to develop.

Healthy individuals may suffer only short-term symptoms such as high fever, severe headaches, stiffness, nausea, abdominal pain and diarrhea. Serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Listeria infection can cause miscarriages and stillbirths among pregnant women.

A number of other products made with sunflower seeds and other ingredients from Hudson Valley Farms have been recalled in recent weeks in the United States and Canada.

Those recalled products include three brands of hummus — Marketside, Lantana and Fresh Foods Market — protein bars, oatmeal and trail mix with organic dates

An FDA spokesman told Food Safety News in June that Hudson Valley Farms has stopped operations and will not restart without prior notice to FDA.

“The FDA is working with Hudson Valley Foods Inc. to facilitate their recall and remove potentially contaminated food from the marketplace. Additionally, the firm is working on corrective actions to remediate the situation and identify the source. We have no further information to share at this time,” said the FDA spokesman.

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One dead, 46 sick in Salmonella outbreak traced to papayas

Federal officials have joined Maryland’s Health Department in a warning against eating yellow Maradol papayas because of Salmonella contamination, reporting one person has died and at least 46 others are sick in an ongoing outbreak that began in mid-May.

The CDC posted this photo with the outbreak notice, describing Maradol papayas as large, oval fruits that weigh 3 or more pounds, with green skins that turn yellow when the fruit is ripe. The flesh inside the fruit is salmon-colored.” Photo courtesy of CDC

Additional victims are likely to be added to the case count because people who became ill after June 23 might not be reported yet because of the lag time between when a person becomes ill and when the illness is recorded by public health officials, according to the Centers for Disease Control and Prevention.

As of 8 p.m. Eastern time Friday no recalls had been posted by the Food and Drug Administration, but the agency is working with the CDC and state officials to investigate the source of the contamination.

The Friday afternoon outbreak investigation announcement from the CDC came on the heels of a Wednesday warning from public health officials in Maryland. The state’s warning specified Caribeña-brand yellow Maradol papayas, but the CDC did not reference brands.

Maryland out in front
Maryland officials began looking at papayas after several people infected by Salmonella bacteria reported eating fresh papayas purchased from a grocery store in Baltimore. Laboratory testing found two strains of Salmonella on the fruit that match strains isolated from sick people who reported eating papayas before becoming ill.

“Salmonella Kiambu and Salmonella Thompson were isolated from samples collected from ill people,” according to the CDC outbreak announcement.

“The Maryland Department of Health collected papayas from the grocery store associated with the illness cluster to test for Salmonella. One sample yielded the outbreak strain of Salmonella Kiambu and another sample yielded Salmonella Thompson. Both samples were from yellow Maradol papayas.

The CDC used whole genome sequencing (WGS) to obtain the DNA fingerprints of the Salmonella strains, which showed the pathogens found on the papayas from the grocery store matched those that infected the outbreak victims.

Advice to consumers, restaurants, retailers
“Based on the available evidence, CDC recommends that consumers not eat, restaurants not serve, and retailers not sell yellow Maradol papayas until we learn more,” according to the outbreak notice.

Additional recommendations from CDC include:

  • If you aren’t sure if the papaya you bought is a yellow Maradol papaya, you can ask the place of purchase. Restaurants and retailers can ask their supplier.
  • When in doubt, don’t eat, sell, or serve them. Throw them out.
  • Wash and sanitize countertops as well as drawers or shelves in refrigerators where papayas were stored.

Anyone who has eaten fresh papaya recently and developed symptoms of Salmonella infection is urged to seek medical attention and tell their doctors about the possible exposure so the proper diagnostic tests can be performed.

Salmonella bacteria can cause diarrhea, vomiting, stomach pain and fever. Symptoms usually begin between 12 to 36 hours after exposure, but they may begin as early as 6 hours or as late as 72 hours after exposure.

Symptoms can be mild or severe and commonly last for two to seven days. Salmonella can infect anyone, but young children, older adults and people with weakened immune systems are the most likely to have severe infections.

Outbreak details
As of July 21, 2017, 47 people infected with the outbreak strain of Salmonella Kiambu have been reported from 12 states.

Illnesses started on dates ranging from May 17 to June 28. Ill people range in age from less than 1 year to 95, with a median age of 27.

Among 33 people with available information, 12, or 36 percent reported being hospitalized. One death has been reported from New York City.

In interviews, ill people answered questions about the foods they ate and other exposures in the week before they became ill. Eleven, or 44 percent, of 25 people interviewed reported eating papayas.

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Tuesday, July 18, 2017

Woodstock brand organic vanilla oats recalled for Listeria risk

Garden of Light Inc., doing business aa Gluten Free Solutions in East Hartford, CT, has joined the list of companies recalling food because it contains ingredients from Hudson Valley Farms Inc., which found Listeria monocytogenes in its facility. Hudson Valley provided an ingredient to Garden of Light, which manufactures the recalled oats for Blue Marble Brands.

Hudson Valley Farms notified Garden of Light of the potential contamination, which already hit several brands, and now includes the recalled “Woodstock Organic Matcha Vanilla Oats.” According to the recall notice posted on the Food and Drug Administration’s Website, no illnesses have been reported to date in connection with this problem.

“The potential contaminated ingredient was thoroughly tested and was negative for Listeria,” according to the recall notice. “The production of the product has been suspended while the company continues to investigate the source of the problem.”

The 1.8-ounce containers subject to the recall were distributed nationwide in retails stores. The paperboard cups have a green laminated film lid. The recalled item, Woodstock Organic Matcha Vanilla Oats, can be identified by checking the product labels for the UPC code 0-42563-01786-6. Consumers can also check for the “SELL BY MAY 11 2018” date on the label.

A second lot with the Best Buy Date Code of “SELL BY JUNE 23 2018” was intercepted before it was released to the general public, according to the recall notice.

Anyone who has eaten the recalled products and developed symptoms of listeriosis should seek medical attention and tell their doctors about the possible exposure. Additionally, anyone who has eaten the above product recently should monitor themselves for symptoms during the coming weeks because it can take up to nine weeks after exposure for symptoms to develop.

Healthy individuals may suffer only short-term symptoms such as high fever, severe headaches, stiffness, nausea, abdominal pain and diarrhea. Serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Listeria infection can cause miscarriages and stillbirths among pregnant women.

Consumers with questions can contact Blue Marble Brands at 888-534-0246.

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Monday, July 17, 2017

Bestherbs Coffee recalled because it contains drug like Viagra

Bestherbs Coffee LLC is recalling all lots of 13-gram packages of “New of Kopi Jantan Tradisional Natural Herbs Coffee” because FDA laboratory analysis confirmed the presence of desmethyl carbodenafil, which is similar to the active ingredient in Viagra and can be deadly when combined with nitrates frequently found in heart and blood pressure medications.

The recall comes almost a year after the Food and Drug Administration posted a public notice on Aug. 30, 2016, warning against the same product, reporting it found desmethyl carbodenafil in the beverage mix, which is marketed as a male enhancement product. Bestherbs Coffee LLC distributed this product from July 2014 through June 2016.

No illnesses had been confirmed in relation to the Bestherbs Coffee product as of the posting of the recall on July 13. However, in May a recall notice of a similar product by Caverflo.com reported one death.

New of Kopi Jantan Tradisional Natural Herbs Coffee also contains milk, which is not declared on the packaging as required by federal law. People who have milk allergies or sensitivities and consume this product, are at risk of serious or life threatening reactions, according to the recall notice posted on the FDA website.

The undeclared desmethyl carbodenafil in the coffee could interact with nitrates in other prescription drugs, such as nitroglycerin. It is common for men with diabetes, high blood pressure, high cholesterol or heart disease to be prescribed nitrates. The undeclared drug could lower blood pressure to dangerous levels.

There is concern consumers may have unused portions of the recalled 13-gram, red packs in their homes. To determine if they have the recalled product, consumers should check the box, which contains 25 packets, for the UPC number 557205060083.

“New of Kopi Jantan Tradisional Natural Herbs Coffee is consumed as an instant coffee. New Kopi Jantan Tradisional Natural Herbs Coffee was distributed nationwide to consumers via individuals or internet,” according to the recall notice

Although no illness has been reported to date, the FDA reported that Bestherbs Coffee is continuing to notify its customers of the recall by phone. Consumers are being urged to discard the product immediately and contact their doctor.

This recall is the most recent in a series of warnings and recalls involving coffee products posted by FDA in the past year, specifically because of undeclared erectile dysfunction drugs:

  • In September 2016 FDA posted a warning about Stiff Bull brand “Herbal Coffee” because it found undeclared desmethyl carbodenafil while inspecting international mail shipments.
  • In May this year Caverflo.com recalled its “Natural Herbal Coffee” after FDA laboratory analysis confirmed the presence of Sildenafil and Tadalafil, which are the active ingredients in two prescription drugs used for the treatment of erectile dysfunction. Caverflo.com has received a report of an individual death after use of the coffee. Caverflo Natural Herbal Coffee may also contain undeclared milk according to the May recall notice.
Health care professionals and patients are encouraged to report adverse events or side effects related to the use of such products to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program:

In its warning notices, the FDA reported “a growing trend of dietary supplements or conventional foods with hidden drugs and chemicals.”

“These products are typically promoted for sexual enhancement, weight loss, and body building and are often represented as being ‘all natural.’ FDA is unable to test and identify all products marketed as dietary supplements that have potentially harmful hidden ingredients,” according to the FDA’s notices warning against the coffee products.

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Saturday, July 15, 2017

7.2 million pounds of hotdogs recalled after oral injury; consumer complaints

Bronx, NY-based Marathon Enterprises Inc.  overnight recalled  approximately 7,196,084 pounds of hot dog products that may be contaminated with extraneous materials, specifically bone fragments, according to the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS).

The contamination  was first reported through the FSIS’ Consumer Compliant Monitoring System (CCMS) on July 10, 2017. Complaints stated that extraneous material, specifically pieces of bone, were found within the product.  CCMS also received on report of a minor oral injury from eating one of the bone-bearing products.

Anyone concerned about an injury or illness should contact a healthcare provider.

The beef and pork hot dog and sausage items were produced on various dates between March 17, 2017 and July 4, 2017. Both retail and institutional products are subject to the recall with the UPC codes referred  to being the last three or four digits of the number in the code.

Retail:

  • 3-lb. package of “SABRETT NATURAL CASING BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 410.
  • 3-lb. package of “SABRETT SKINLESS BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 414.
  • 14-oz. package of “BUN SIZE SABRETT SKINLESS BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 416.
  • 14-oz. package of “SABRETT SKINLESS BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 417.
  • 12-oz. package of “SABRETT NATURAL CASING BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 428.
  • 14-oz. package of “NEW SABRETT ALL NATURAL SKINLESS UNCURED BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 437.
  • 3-lb. package of “SABRETT ALL NATURAL SKINLESS UNCURED BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 438.
  • 40-oz. package of “SABRETT ALL NATURAL SKINLESS UNCURED BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 439.
  • 14-oz. package of “Western Beef THE MEAT SUPERMARKET BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 451.
  • 16-oz. package of “SABRETT HOT SUSAGE” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 479.
  • 14-oz. package of “Jalapeno SABRETT SPICY HOT & SPICY BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 480.
  • 80-oz. package of “ABOUT 50 BEEF FRANKS SABRETT SKINLESS BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 644.
  • 48-oz. package of “ABOUT 30 BEEF FRANKS SABRETT SKINLESS BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 732.
  • 40-oz. package of “ABOUT 25 BEEF FRANKS SABRETT SKINLESS BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 738.
  • 32-oz. package of “ABOUT 20 BEEF FRANKS SABRETT SKINLESS BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 740.
  • 80-oz. package of “SABRETT SKINLESS BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 743.
  • 32-oz. package of “SABRETT 78-82 Pieces SKINLESS BEEF COCKTAIL FRANKS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 754.
  • 12-oz. package of “APPROXIMATELY 30 PIECES SABRETT SKINLESS BEEF COCKTAIL FRANKS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 771.
  • 12-oz. package of “APPROXIMATELY 30 PIECES SABBRETT BRATWURST SKINLESS BEEF & PORK COCKTAIL FRANKS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017. And UPC code 772.
  • 12-oz. packages of Sabrett brand “APPROXIMATELY 30 PIECES SABRETT BEEF & CHEDDAR SKINLESS BEEF COCKTAIL FRANKS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 773.
  • 12-oz. package of “APPROXIMATELY 30 PIECES SABRETT ALL NATURAL SKINLESS BEEF COCKTAIL FRANKS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 UPC code 774.
  • 48-oz. package of “SABRETT HOT SAUSAGE” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 779.
  • 16-oz. packages of Stew Leonard’s.com brand “beef franks” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017.
  • Various weights and sizes of “PAPAYA KING BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 1420 and 1421.
  • 14-oz. package of “1906 PREMIUM * BEEF FRANKS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 1906.
  • 2.5-lb. package of “1906 PREMIUM * BEEF FRANKS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 3860.
  • 12.5-oz. package of “24 PIECES SABRETT COCKTAIL FRANKS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 761.
  • 1-lb. 9-oz. package of “48 PIECES SABRETT COCKTAIL FRANKS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 762.
  • Various weights and sizes of “SABRETT Exclusively for Wind Mill Natural Casing HOT DOGS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017.

Institutional

  • Various weights and sizes of “SABRETT NATURAL BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 with UPC codes 530, 601, 602, 603, 604, 605, 606, 607, 666, 682, 725, 1065, 1201, 1420, 1421, 1530, 1603, 1699, and 1899.
  • Various weights and sizes of “Nathan’s Private Label” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC code 618.
  • Various weights and sizes of “SABRETT SKINLESS BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 and UPC codes 400, 437, 451, 455, 480, 630, 637, 638, 639, 640, 735, 736, 745, 748, 749, 750, 753, 754, 756, 757, 758, 759, 761, 762, 768, 770, 771, 773, 774, 800, 1012, 1013, 1040, 1060, 1061, 1062, 1064, 1066, 1101, 1438, 1440, 1441, 1480, 1637, 1638, 1639, 1644, 1735, 1748, 1756, 1999,2417, and 3860.
  • Various weights and sizes of “SABRETT NATURAL CASING PORK AND BEEF FRANKFURTERS” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 with UPC codes 510, 511, 512, 514, 515, 520, 521, 550, and 2403.
  • Various weights and sizes of “SABRETT SKINLESS PORK AND BEEF FRANKFURTER” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 with UPC codes 554, 590, 592, 593, 596, 772, and 1100.
  • Various weights and sizes of “SABRETT HOT SAUSAGE” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 with UPC codes 479, 778, 779, and 786.
  • Various weights and sizes of “KATZ’S DELICATESSEN Salami” with a use by/sell by date between June 19, 2017 and Oct. 6, 2017 with UPC codes 950, 951, 952, 953, and 954.

The products subject to recall bear establishment number “EST. 8854” inside the USDA mark of inspection. These items were shipped to retail and institutional locations nationwide.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website.

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Friday, July 14, 2017

Importer recalls ground cumin after NY inspectors find lead

A New York import-export company is recalling an undisclosed volume of ground cumin because it was found to be contaminated with lead.

Sol Andino Import & Export of Jackson Heights, NY, distributed the ground cumin to retail stores in New York, New Jersey and Connecticut, according to the recall notice.

Consumers can identify the recalled product, which is packaged in 2-ounce plastic bags, by looking for the UPC number 884752003812. No other traceability information was provided in the recall notice. The notice did not include product photos.

“The contamination was discovered after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of excessive levels of lead in some 2-ounce packages of the ‘Ground Comin’ (Ground Cumin),” according to the recall notice posted July 10 on the department website.

“Distribution of the product has been suspended while the company continues their investigation to find the source of the problem.”

The lead levels measured in the recalled cumin are high enough to cause health problems — particularly in infants, small children, pregnant women, and those with underlying kidney disorders, according to New York officials.

If a child or a pregnant woman is exposed to lead, permanent damage can be caused to the central nervous system. Children can develop learning disorders, developmental defects, and other long-term health problems.

“Pregnant women, children and patients with underlying kidney problems who may have consumed this product should consult with their physician or health care provider,” according to the recall notice.

Anyone who has purchased the recalled cumin is urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company Sol Andino Import & Export at 917-288-4704.



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Silver Star Chipotle Queso Dip recalled for undeclared cheese, milk & eggs

Austin’s Texas Legend Foods has its 16 ounce jars of Silver Star Chipotle Queso Dip because they contain undeclared cheese, milk and eggs. People who have allergies to cheese, milk and eggs run the risk of a serious or life-threatening allergic reaction if they consume this product.

The recalled “Silver Star Chipotle Queso Dip” was distributed nationwide in retail stores.

The product comes in a 16 ounce clear glass jar marked with one of the following Lot #’s: 060AFV7A, 072AFV7A, 072AFV7B, 090AFV7A, 111AFV7A which is stamped on the top of the glass jar beneath the lid. UPC CODE #819993005394

No illnesses have been reported to date in connection with the recalled products.

The recall was initiated after it was discovered that the milk, cheese and egg containing product was distributed in packaging that did not reveal the presence of the milk, cheese and egg. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company’s production and packaging processes.

Production of the product has been suspended until FDA and the company are certain that the problem has been corrected.  Consumers who have purchased jars of “Silver Star Chipotle Queso Dip” are urged to return them to the place of purchase for a full refund.

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Mislabeling and undeclared allergens spark base products recall

Oswego, IL-based Custom Culinary, Inc. is recalling approximately 9,444 pounds of chicken and beef base products due to misbranding and undeclared allergens, according to  the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS). The products’ labels incorrectly identified the products as chicken, but may contain beef. Additionally, the products contain soy, a known allergen, which is not declared on the product label.

The chicken and beef soup base items were packaged on May 25, 2017.  Subject to recall are:

  •   6-lb. corrugate case “Molly’s Kitchen Soup Base Paste Beef Base Paste – NO MSG Added with a lot code of 72505 239497 or 72505 239498.
  • 1-lb. white plastic jars of “Molly’s Kitchen Chicken Base Paste / 301817 / No MSG Added with a lot code of 72505 239497 or 72505 239498

The products subject to recall bear establishment number “EST. 2016” or “EST. P-1278” inside the USDA mark of inspection. These items were shipped to food service distributors nationwide.

The mistake was discovered when one of the company’s foodservice distributors was notified that a customer had received a case of product with mislabeled jars. The jar received was a beef base labeled as chicken base.

No confirmed reports of adverse reactions have been associated with the recalled products.  Anyone concerned about an injury or illness should contact a healthcare provider.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website.



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Thursday, July 13, 2017

CFIA adds brand, additional lots to butter recall for Listeria

No illnesses have been confirmed, but Canadian officials have again expanded a recall of butter because of positive test results for Listeria monocytogenes, adding a fourth brand and 10 more lots or previously recalled brands.

The new recall, posted late Tuesday by the Canadian Food Inspection Agency (CFIA), adds the Nutrinor brand to the list that already included St Laurent, Perron and Beurre du Lac branded butter. None of the recall notices provide any details on the dairy or dairies involved or any manufacturing details.

“Industry is recalling various brands of butter from the marketplace due to possible Listeria monocytogenes contamination,” according to the latest CFIA recall notice.

“Consumers should not consume the recalled products… Food contaminated with Listeria monocytogenes may not look or smell spoiled but can still make you sick.”

Because of the long shelf live of butter, there is concern that consumers could have unused portions of the recalled butter in their homes. Products that are on the following recall list should be thrown away immediately, or returned to the store where they were purchased, according to the CFIA.

Consumers can identify the recalled butter by looking for the following information printed on the packaging:

  • Perron brand butter in 454-gram packages with the product code 143 069 and the UPC number 7 72622 72454 0;
  • Beurre du Lac brand butter in 454-gram packages with the product codes 102 024, 107 025, 122 029, 128 030, 135 031 or 149 033 and the UPC number 0 62260 00455 6;
  • St-Laurent brand butter in 454-gram packages with the product codes 110 050, 122 058, 122 059, 125 061, 125 062 or 128 064 and the UPC number 0 62260 00454 9; and
  • Nutrinor brand butter in 454-gram packages with the product codes 122 057, 122 058, 125 060, and 125 061 and the UPC number 0 65244 45827 7.

Anyone who has eaten any of the recalled butter and developed symptoms of listeriosis should seek medical attention and tell their doctors about the possible exposure to Listeria so the proper diagnostic tests can be performed.

Also, people who have eaten the recalled butter recently should monitor themselves during the coming weeks because it can take up to 70 days after exposure for symptoms to appear.

“Symptoms can include vomiting, nausea, persistent fever, muscle aches, severe headache and neck stiffness. Pregnant women, the elderly and people with weakened immune systems are particularly at risk,” according to the CFIA recall notice.

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Wednesday, July 12, 2017

Loblaw’s recalls chicken nuggets linked to Salmonella outbreak

Sixteen days after public health officials in Canada revealed they have been investigating a Salmonella outbreak linked to frozen, raw chicken products the country’s food safety agency posted a recall of President’s Choice brand chicken nuggets.

The Public Health Agency of Canada posted its outbreak notice on June 26 warning consumers about the dangers of undercooked chicken and reporting for the first time a Salmonella outbreak that sickened people in at least four provinces in April and May.

Wednesday the Canadian Food Inspection Agency, which had previously refused to name the implicated products, posted a recall notice stating Loblaw Companies Ltd. is pulling its President’s Choice “Pub Recipe Chicken Nuggets” from stores nationwide because of possible Salmonella contamination.

Consumers can identify the 800-gram packs of “uncooked breaded cutlettes” by looking for the following label information:

  • UPC number 0 60383 13171 5
  • Date code “2018 MR 15”

Officials are concerned consumers may have unused portions of the frozen, raw chicken nuggets in their homes because of the product’s long shelf life.

“Check to see if you have recalled products in your home. Recalled products should be thrown out or returned to the store where they were purchased,” according to the CFIA recall notice.

“Food contaminated with Salmonella may not look or smell spoiled but can still make you sick. Young children, pregnant women, the elderly and people with weakened immune systems may contract serious and sometimes deadly infections. Healthy people may experience short-term symptoms such as fever, headache, vomiting, nausea, abdominal cramps and diarrhea. Long-term complications may include severe arthritis.”

The CFIA reported its investigation is ongoing, adding that additional products could be recalled. As of Wednesday night, neither the Public Health Agency of Canada nor the country’s federal health department Canada Health had posted an update on the outbreak.

In the June 26 outbreak notice the government reported there were at least seven confirmed cases of Salmonella infections at that point. Alberta had four confirmed cases while one case had been confirmed in each of British Columbia, Ontario and New Brunswick.

No deaths have been reported, but two of the seven outbreak victims were so sick they required hospitalization.

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Saturday, July 8, 2017

CFIA recalls two more brands of butter because of Listeria

Government tests that returned positive results for Listeria monocytogenes triggered the recall of two more brands of butter by the Canadian Food Inspection Agency on Saturday, following the Wednesday recall of St Laurent brand butter.

As with the St Laurent butter, the recalled Perron brand and Beurre du Lac brand butter was sold by retailers in the province of Quebec, according to the recall notice on the CFIA website.

“This additional information was identified during the CFIA food safety investigation,” according to the recall notice. “Consumers should not consume the recalled products described below.

“Check to see if you have recalled products in your home. Recalled products should be thrown out or returned to the store where they were purchased. Food contaminated with Listeria monocytogenes may not look or smell spoiled but can still make you sick.”

Consumers can identify the butter added to the recall by looking for the following information printed on the packaging:

  • Perron brand butter in 454-gram packages with the product code 143 069 and the UPC number 7 72622 72454 0; and
  • Beurre du Lac brand butter in 454-gram packages with the product code 143 032 and the UPC number 0 62260 00455 6.

Anyone who has eaten any of the recalled butter and developed symptoms of listeriosis should seek medical attention and tell their doctors about the possible exposure to Listeria so the proper diagnostic tests can be performed. Also, people who have eaten the recalled butter recently should monitor themselves during the coming weeks because it can take up to 70 days after exposure for symptoms to appear.

“Symptoms can include vomiting, nausea, persistent fever, muscle aches, severe headache and neck stiffness. Pregnant women, the elderly and people with weakened immune systems are particularly at risk,” according to the CFIA recall notice.

“Although infected pregnant women may experience only mild, flu-like symptoms, the infection can lead to premature delivery, infection of the newborn or even stillbirth. In severe cases of illness, people may die.”

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Wednesday, July 5, 2017

CLIF bars recalled after consumers report allergic reactions

Cliff Bar & Co. is recalling three flavors of granola bars — two marketed as children’s products — because of undeclared nuts and consumer complaints about allergic reactions.

The product labels do not declare the presence of peanuts or tree nuts, but the CLIF Builder’s bars and CLIF Kid Zbars may contain peanuts, almonds, Brazil nuts, cashews, hazelnuts, macadamia nuts, pecans, walnuts or coconuts, according to the recall notice posted Wednesday on the Food and Drug Administration’s website.

Retailers Trader Joe’s and Stop & Shop posted their own recall notices for the Clif Bar & Co. products. All of the recall notices warn that people with allergies or sensitivities to peanuts or tree nuts should not eat the recalled bars.

“People with an allergy to peanuts and these specific tree nuts run the risk of a serious or life-threatening allergic reaction. The company is strongly advising consumers who have peanut and these specific tree nut allergies not to consume these bars,” according to the recall notice on the FDA website.

“The affected products are sold in retail stores and online throughout the U.S.

Clif Bar discovered this issue when it received a small number of consumer complaints alleging peanut or tree nut allergic reactions.”

The company is asking consumers to return the recalled products to the store where they were purchased to request an exchange or full refund. Affected product should then be discarded in a secure place and not consumed, according to the recall notice.

The specific CLIF bars subject to this recall can be identified by the following label information:

  • CLIF Builder’s 18-count variety packs of Chocolate Peanut Butter and Chocolate Mint with the Lot Code “FROM: 24MAR16M” and the Lot Code “TO: 08FEB18M”
  • CLIF Kid Zbar Protein 30-count variety packs with the Lot Code “FROM: 31MAY16M” and the Lot Code “TO: 15OCT17M”
  • CLIF Builder’s Chocolate Mint 12-pack with the Lot Code “FROM: 05APR16M3” and the Lot Code “TO: 23APR18M3”
  • CLIF Builder’s Chocolate Mint 6-pack with the Lot Code “FROM: 05APR16M3” and the Lot Code “TO: 23APR18M3”
  • CLIF Builder’s Chocolate Mint 7-pack with the Lot Code “FROM: 05APR16M3” and the Lot Code “TO: 23APR18M3”
  • CLIF Builder’s Snack Size Chocolate Mint 200-count with the Lot Code “FROM: 05APR16M3” and the Lot Code “TO: 23APR18M3”
  • CLIF Kid ZBar Protein Chocolate Chip 10-pack with the Lot Code “FROM: 05APR16M3” and the Lot Code “TO: 23APR18M3”
  • CLIF Kid ZBar Protein Chocolate Chip 150-count with the Lot Code “FROM: 05APR16M3” and the Lot Code “TO: 23APR18M3”
  • CLIF Kid Zbar Protein Chocolate Chip 5-pack with the Lot Code “FROM: 05APR16M3” and the Lot Code “TO: 23APR18M3”
  • CLIF Kid Zbar Protein Chocolate Mint 10-pack with the Lot Code “FROM: 05APR16M3” and the Lot Code “TO: 23APR18M3”
  • CLIF Kid ZBar Protein Chocolate Mint 150-count with the Lot Code “FROM: 05APR16M3” and the Lot Code “TO: 23APR18M3”
  • CLIF Kid Zbar Protein Chocolate Mint 5-pack with the Lot Code “FROM: 05APR16M3” and the Lot Code “TO: 23APR18M3”

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Canadian test finds Listeria in St Laurent butter; recall initiated

Government inspectors found Listeria monocytogenes in a sample of St Laurent brand butter, spurring the company Maurice St-Laurent Limitée to recall an undisclosed amount of the butter.

“Check to see if you have recalled product in your home. Recalled product should be thrown out or returned to the store where it was purchased,” according to the recall notice posted Wednesday by the Canadian Food Inspection Agency.

“Food contaminated with Listeria monocytogenes may not look or smell spoiled but can still make you sick.”

The company reported distributing the recalled St Laurent brand butter to retailers in the province of Quebec.

Consumers can identify the recalled butter by looking for the following label information: St Laurent butter in 454-gram packages with the product code 156 074 and the UPC number 0 62260 00454 9.

Anyone who has eaten any of the recalled butter and developed symptoms of Listeria infection should seek medical attention and tell their doctors about the possible exposure so the proper diagnostic tests can be done.

Also, since it can take up to 70 days for symptoms of listeriosis to develop, anyone who has eaten any of the recalled butter is urged to monitor themselves for symptoms during the coming weeks.

Symptoms can include vomiting, nausea, persistent fever, muscle aches, severe headache and neck stiffness. Pregnant women, the elderly and people with weakened immune systems are particularly at risk. Although infected pregnant women may experience only mild, flu-like symptoms, the infection can lead to premature delivery, infection of the newborn or even stillbirth. In severe cases of illness, people may die.

No illnesses had been reported in connection to the recalled butter as of the posting of the recall notice. The CFIA is investigating the source of the Listeria contamination and may post additional recalls.

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Tuesday, July 4, 2017

Evanger’s proposes donating recalled pet food. FDA says ‘no’

The United States Food and Drug Administration (FDA) has vetoed a proposal by Evanger’s Dog and Cat Food Co. to donate recalled pet food to animal shelters after conducting random spot-checks for pentobarbital.

The proposal was revealed in a June 29, 2017 Warning Letter issued by FDA, and released on its website Tuesday morning (July 4, 2017) under the agency’s standing policy to post recent Warning Letters on a weekly basis.

The letter addressed to Holly N. Sher and Joel A. Sher, President and Vice President, respectively, notifies them that FDA found “…serious violations of the Federal Food, Drug, and Cosmetic Act (FD&C Act) and its implementing regulations” during an investigation that included supplier traceback, facility inspection, and analysis of samples collected by FDA.

In its response to the Evanger’s proposal to donate recalled pet food, FDA said that finding the contents of individual cans of food from recalled lots to be negative for pentobarbital would not provide “…sufficient assurance that the remaining units are not adulterated.”

After stating that FDA’s own testing confirmed the pentobarbital contamination not to be homogeneous throughout an entire lot, the agency declined Evanger’s proposal and recommended destruction of all remaining recalled product.

The Warning Letter is the most recent development in an investigation of Evanger’s that began in early January with the reported illness of five dogs in a single household and the death of one of the dogs. Lab tests conducted on the gastric contents of the dead dog and on the remains of Evanger’s Hunk of Beef au Jus canned dog food that had been fed to all five of the animals, revealed the presence of a ‘large quantity’ of pentobarbital in both samples.

FDA opened its investigation immediately upon becoming aware of the incident. A team of inspectors began an on-site inspection of Evanger’s manufacturing facility in Wheeling, Illinois on January 10, 2017.

On February 14, 2017, the inspection team furnished Evanger’s management with a Form 483, listing a series of Inspectional Observations, including:

• Pentobarbital found in a sample of Evanger’s Hand Packed Hunk of Beef au Jus, 12 oz. can (Lot #1816E06HB13)

• Pentobarbital found in a sample of Against the Grain brand Grain Free Pulled Beef with Gravy Dinner for Dogs, 12 oz. can (Lot #2415E01ATB12; BEST DEC 2019)

• Condensate dripping throughout the facility, including into open cans in-process and onto totes of raw meat

• Pitted, cracked and damaged floors

• Peeling paint, mold throughout the facility and a live ‘fly-like insect’ in the hand-packing area during processing

• Inadequate temperature controls

In addition to the two pentobarbital-positive samples cited in the February 14th Form 483, FDA has found pentobarbital in the following five production lots of Evanger’s dog food:

• Braised Beef Chunks, lot code 2016E08BBW11 Best Aug 2020.

• Hunk of Beef Au Jus, lot code 1816E14HBC18 Best June 2020.

• Hunk of Beef Au Jus, lot code 1816E02HB12 Best June 2020.

• Hunk of Beef Au Jus, lot code 1316E23HB09 Best Jan 2020.

• Hunk of Beef Au Jus, lot code 1816E03HB17 Best June 2020.

On March 3, 2017, Evanger’s voluntarily recalled all cans of Evanger’s Braised Beef Chuncks, Evanger’s Hunk of Beef Au Jus and Against the Grain Pulled Beef with Gravy manufactured between December 2015 and January 2017.

In correspondence dated 2/4/2017, 2/21/2017, 4/4/2017, 5/18/2017 and 5/23/2017, Evanger’s addressed FDA’s Inspectional Observations, and proposed a series of corrective actions. In addition to the proposed donation of recalled product, the following actions, listed in the Warning Letter, are those FDA found to be inadequate or unacceptable.

Evanger’s discontinued doing business with the meat supplier alleged by the company to be the source of the adulterated meat.

Evanger’s was unable to supply any documentation or evidence that the indicated supplier was the only one who supplied the contaminated raw materials. Therefore, FDA was unable to evaluate whether or not this was an adequate response.

Evanger’s suggested that if pentobarbital were to be present in any of its ground loaf products, it would be “…well within the range that FDA had previously deemed not to be a health or safety concern in pet foods.”

FDA disagrees that grinding would dilute any pentobarbital to safe levels, and points out that there is zero tolerance for pentobarbital in pet food.

Evanger’s proposed random pentobarbital tests of finished products prior to shipment as a way to ensure that raw materials are not adulterated.

FDA considers this to be an inadequate and unreliable way to ensure the safety of the finished product. FDA’s own testing has demonstrated pentobarbital contamination is not uniformly distributed throughout all cans in a production lot. Also, the agency disagrees that finished product testing can mitigate the risk of pentobarbital in the raw material.

Evanger’s now requires new and current suppliers to provide letters of guarantee for their products.

FDA points out that a letter of guarantee may not provide adequate assurance of product safety, and recommends conducting site audits and/or reviews of supplier procedures in addition to the letter of guarantee.

As is customary, the Warning Letter concludes with a requirement that Evanger’s must furnish a written reply within fifteen working days, spelling out the steps it has taken or will take to correct the violations and prevent them from occurring again.

The complete text of the Warning Letter can be found on the FDA website.

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