The #FDA Investigates Multistate Outbreak of #Ecoli O121 Infections Linked to #Flour

FDA Investigates Multistate Outbreak of E. coli O121 Infections Linked to Flour

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Update: July 1, 2016

The U.S. Food and Drug Administration (FDA) along with the Centers for Disease Control and Prevention (CDC) and state and local officials are investigating a multi-state outbreak of Shiga toxin-producing Escherichia coli O121 (STEC O121) infections.
On July 1, 2016, following a call with the FDA and CDC, General Mills expanded its recall of Gold Medal flour, Wondra flour, and Signature Kitchens flour.
Testing by FDA has now identified E. coli O121 in open product samples collected from ill people in Arizona and Oklahoma. FDA whole genome sequencing of the E.coli O121 isolate from the Arizona product sample is closely genetically related to the outbreak strain. Pulsed-field gel electrophoresis (PFGE) shows that the Oklahoma product sample isolates match the outbreak strain. The General Mills flour sample collected from the Oklahoma patient was purchased outside of the company’s original recall date range.
What is the Problem and What is Being Done About It?  
The FDA, CDC and state and local officials are investigating a multi-state outbreak of Shiga toxin-producingEscherichia coli O121 (STEC O121) infections.
The CDC reports that 42 people infected with the outbreak strain of E. coli O121 have been reported from 21 states. Illnesses started on dates ranging from December 21, 2015 to June 8, 2016. Eleven ill people have been hospitalized. In its investigation, CDC learned that some people who got sick had eaten or handled raw dough.
FDA’s traceback investigation determined that the raw dough eaten or handled by ill people or used in restaurant locations was made using General Mills flour that was produced in November 2015 at the General Mills facility in Kansas City, Missouri. Epidemiology, laboratory and traceback evidence available at this time indicate that General Mills flour manufactured at this facility is the likely source of the outbreak.
On May 31, 2016, following a conference call among FDA, CDC and the firm, General Mills conducted avoluntary recall of flour products produced between November 14, 2015 and December 4, 2015. Recalled products are sold in stores nationwide or may be in consumers’ pantries and are sold under three brand names: Gold Medal flour, Signature Kitchens flour and Gold Medal Wondra flour. The varieties include unbleached, all-purpose, and self-rising flours.
On June 10, 2016, FDA whole genome sequencing on E. coli O121 isolates recovered from an open sample of General Mills flour belonging to a Colorado consumer who was sickened was found to be closely genetically related the clinical isolates from human illnesses. The flour came from a lot that General Mills has recalled.
Testing by FDA has now identified E. coli O121 in open product samples collected from ill people in Arizona and Oklahoma. FDA whole genome sequencing of the E.coli O121 isolate from the Arizona product sample is closely genetically related to the outbreak strains Pulsed-field gel electrophoresis (PFGE) shows that the Oklahoma product sample isolates match the outbreak strain. The General Mills flour sample collected from the Oklahoma patient was purchased outside of the company’s original recall date range.
On July 1, 2016, following a call with the FDA and CDC, General Mills expanded its recall of Gold Medal flour, Wondra flour, and Signature Kitchens flour.
General Mills also sells bulk flour to customers who use it to make other products. General Mills has contacted these customers directly to inform them of the recall. FDA is working with General Mills to ensure that the customers have been notified, and to evaluate the recall for effectiveness. Because of legal restrictions on disclosure of commercial confidential information, FDA is not at this time authorized to release the names of these customers or the products they make with the flour.
Flour has a long shelf life, and bags of flour may be kept in peoples’ homes for a long time. Consumers unaware of the recall could continue to eat these recalled flours and potentially get sick. If consumers have any of these recalled flours in their homes, they should throw them away.
The investigation is ongoing and FDA will provide updated information as it becomes available. 
What are the Symptoms of E.coli O121?
People usually get sick from STEC O121 2-8 days (average of 3-4 days) after swallowing the bacteria. Most people develop diarrhea (often bloody) and abdominal cramps. Most people recover within a week.
Some illnesses last longer and can be more severe, resulting in a type of kidney failure called hemolytic uremic syndrome (HUS). HUS can occur in people of any age, but is most common in young children under 5 years, older adults, and people with weakened immune systems.
Symptoms of HUS can include fever, abdominal pain, pale skin tone, fatigue and irritability, small, unexplained bruises or bleeding from the nose and mouth, and decreased urination.
People who experience these symptoms should seek emergency medical care immediately.
Who is at Risk?
People of any age can become infected. Very young children and the elderly are more likely than others to develop severe illness and HUS, but even healthy older children and young adults can become seriously ill.
What Specific Products are Being Recalled? 
Recalled products are currently sold in stores or may be in consumers’ pantries and are sold under three brand names: Gold Medal Flour, Signature Kitchens Flour, and Gold Medal Wondra flour. The recalled products were sold nationwide and include unbleached, all-purpose, and self-rising flours varieties.
On July 1, 2016, General Mills issued an expanded recall to include 8 SKUs (stock keeping units or UPC codes) of Gold Medal Flour, 1 SKU of Signature Kitchens Flour and 1 SKU of Gold Medal Wondra flour. Consumers, restaurants, and retailers do not use, serve, or sell the recalled flours.
The specific products in the recall include: 
13.5oz Gold Medal Wondra Flour
Package UPC
000-16000-18980
Recalled Better if Used by Dates
25FEB2017 thru 30MAR2017
Added July 1, 2016:
23FEB2017KC, 24FEB2017KC
2lb Gold Medal All Purpose Flour
Package UPC
000-16000-10710
Recalled Better if Used by Dates
25MAY2017KC thru 03JUN2017KC
Added July 1, 2016:
15MAY2017KC through 24MAY2017KC, 04JUN2017KC, 05JUN2017KC, 11JUN2017KC, 12JUN2017KC, 13JUN2017KC, 14JUN2017KC 
2lb Gold Medal Self-Rising Flour
Package UPC
000-16000-11710
Recalled Better if Used by Dates
23AUG2016KC
Added July 1, 2016:
09AUG2016KC, 10AUG2016KC, 16AUG2016KC, 17AUG2016KC, 06SEP2016KC, 07SEP2016KC
10lb Gold Medal All Purpose Flour
Package UPC
000-16000-10410
Recalled Better if Used by Dates
02JUN2017KC,  03JUN2017KC
Added July 1, 2016:
16MAY2017KC through 20MAY2017KC, 05JUN2017KC

5lb Gold Medal All Purpose Flour

Package UPC
000-16000-10610
Recalled Better if Used by Dates
25MAY2017KC, 27MAY2017KC thru 31MAY2017KC, 01JUN2017KC, 03JUN2017KC thru 05JUN2017KC, 11JUN2017KC thru 14JUN2017KC
Added July 1, 2016:
15MAY2017KC through 24MAY2017KC
5lb Gold Medal Unbleached Flour
Package UPC
000-16000-19610
Recalled Better if Used by Dates
25MAY2017KC, 27MAY2017KC, 03JUN2017KC, 04JUN2017KC
Added July 1, 2016:
19MAY2017KC through 24MAY2017KC, 11JUN2017KC, 12JUN2017KC
Added July 1, 2016
5lb Gold Medal Self-Rising Flour
Package UPC
000-16000-11610
Recalled Better if Used by Dates
10AUG2016KC, 11AUG2016KC
Added July 1, 2016
4.25lb Gold Medal All Purpose Flour
Package UPC
000-16000-12670
Recalled Better if Used by Dates
21MAY2017KC, 03JUN2017KC
10lb Gold Medal All Purpose Flour- Banded Pack
Package UPC
000-16000-10410
Recalled Better if Used by Dates
03JUN2017KC, 04JUN2017KC, 05JUN2017KC
Added July 1, 2016
10lb Gold Medal All Purpose Flour- Banded Pack
Package UPC
000-16000-10650
Recalled Better if Used by Dates
15MAY2017KC
5lb Signature Kitchens All Purpose Flour Enriched Bleached
Package UPC
000-21130-53001
Recalled Better if Used by Dates
BB MAY 28 2017
5lb Signature Kitchens Unbleached Flour All Purpose Enriched
Package UPC
000-21130-53022
Recalled Better if Used by Dates
BB MAY 27 2017
Added July 1, 2016
2lb Signature Kitchens All Purpose Flour Enriched Bleached
Package UPC
000-21130-53000
Recalled Better if Used by Dates
BB MAY 27 2017
What Do Restaurants and Retailers Need To Do?
Restaurants and retailers should throw away any recalled General Mills flour. Some ill people reported handling raw dough at restaurants prior to eating their meal. Restaurants that allow their customers to handle raw dough should evaluate whether this practice is appropriate.
Restaurants and retailers should be aware that flour may be a source of pathogens and should control the potential for cross-contamination of food processing equipment and the food processing environment. They should follow the steps below:
  • Wash and sanitize display cases and refrigerators where potentially contaminated products were stored.
  • Wash and sanitize cutting boards, surfaces, and utensils used to prepare, serve, or store potentially contaminated products.
  • Wash hands with hot water and soap following the cleaning and sanitation process.
  • Retailers, restaurants, and other food service operators who have processed and packaged any potentially contaminated products need to be concerned about cross contamination of cutting surfaces and utensils through contact with the potentially contaminated products.
  • Regular frequent cleaning and sanitizing of food contact surfaces and utensils used in food preparation may help to minimize the likelihood of cross-contamination. 
What Do Consumers Need To Do? 
The recalled General Mills products have a long shelf-life, and they may be in peoples’ homes. Consumers unaware of the recall could continue to eat these products and potentially get sick.
If consumers have these products in their homes, they should throw it away. As a precaution, flour no longer stored in its original packaging should be discarded if it could be covered by this recall, and the containers used to store this flour should be thoroughly washed and sanitized.
Three people who became ill reported handling raw dough at restaurants prior to eating their meal. As a precaution, consumers, especially children, should not handle raw dough at home or at restaurant locations.
FDA warns against eating raw dough products made with any brand of flour or baking mix before cooking. Consumers should always practice safe food handling and preparation measures when handling flour. The FDA recommends following these safe food-handling practices to stay healthy:
  • Do not eat or play with any raw cookie dough or any other raw dough product made with flour that is intended to be cooked or baked.
  • Follow package directions on baking mixes and other flour-containing products for proper cooking temperatures and for specified times.
  • Wash hands, work surfaces, and utensils thoroughly after contact with raw dough products containing flour.
  • Keep raw foods separate from other foods while preparing them to prevent any contamination that might be present from spreading.
Who Should be Contacted?
Contact your healthcare provider if you have diarrhea that lasts for more than 3 days, or is accompanied by high fever, blood in the stool, or so much vomiting that you cannot keep liquids down and you pass very little urine.
Consumers with additional questions should contact the company at 800-230-8103. Additional recall information can also be found at www.generalmills.com/flour disclaimer icon.  
The FDA encourages consumers with questions about food safety to call 1-888-SAFEFOOD Monday through Friday between 10 a.m. and 4 p.m. Eastern time, or to consult the fda.gov website: www.fda.gov.
The information in this release reflects the FDA’s best efforts to communicate what it has learned from the manufacturer and the state and local public health agencies involved in the investigation. The agency will update this page as more information becomes available.
Additional Information

New #foodsafety #recall possible residue #adulteration of 21,521 lbs of #Catfish from Haring Catfish, Inc.

Haring Catfish, Inc. Recalls Siluriformes Fish Products Due To Possible Adulteration

Class II Recall060-2016
Health Risk: LowJul 14, 2016
Congressional and Public Affairs 
Benjamin Bell
(202) 720-9113
Press@fsis.usda.gov
WASHINGTON, July 14, 2016 – Haring Catfish, Inc., a Wisner, La. establishment, is recalling approximately 21,521pounds of siluriformes fish (catfish) products that may be adulterated with a residue of public health concern, specifically gentian (crystal) violet, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The siluriformes (catfish) products items were produced on June 28 and 29, 2016. The following products are subject to recall: [View Labels (PDF Only)]
  • 11-lb. Cardboard boxes of IQF (Individually Quick Frozen) “catfish” tails in plastic wrapping identified as HARING CATFISH and having Lot Code 2140 printed on the label.
  • 15-lb. Cardboard boxes of IQF “catfish” steaks, irregular filets, whole fish, strips, nuggets, and partially gutted fish in plastic wrapping identified as HARING CATFISH and having Lot Code 2140 printed on the label.
  • 30-lb. Cardboard boxes of IQF “catfish” steaks, irregular filets, whole fish, strips, nuggets, and partially gutted fish in plastic wrapping identified as HARING CATFISH and having Lot Code 2140 printed on the label.
The products subject to recall bear establishment number “EST. 51217” inside the USDA mark of inspection. These items were shipped to retail locations and hotels, restaurants, and institutions in Arkansas, California, Louisiana, Mississippi, Oklahoma, and Texas.
The problem was discovered on July 11, 2016, after routine FSIS sampling results revealed a violative level of the chemical gentian (crystal) violet in the product.
There have been no confirmed reports of adverse reactions, injury, or illness 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 at www.fsis.usda.gov/recalls.
Consumers with questions about the recall can contact Dottie Walker, at (318) 724-6133 ext. 119. Media with questions about the recall can contact Dawn Payne, at (318) 724-6654.

New #foodsafety #recall #undeclared #egg #allergen in Poppers Brand Mozzarella Cheese Sticks

Monogram Appetizers Issues Allergy Alert On Undeclared (Egg) In Poppers Brand Mozzarella Cheese Sticks

July 14, 2016

Contact

Consumers

Monogram Foods
 1-855-556-1351

Media

DeWayne McVey
 901-259-6642

Announcement

Monogram Appetizers of Plover, Wisconsin is recalling approximately 5000 cases of Poppers Brand Mozzarella Cheese Sticks, because it may contain undeclared egg. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume these products.
The recalled Poppers Brand Mozzarella Cheese Sticks were distributed nationwide in retail stores. The product comes in a 32 ounce, clear plastic package marked with UPC 4670488920 and code numbers.
No illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered that the product was distributed in packaging that did not reveal the presence of egg. The problem was discovered during a routine quality check, which revealed that egg was inadvertently omitted during a recent graphics change.
The use of this product packaging has been suspended and placed on Hold.
Consumers who have purchased 32 ounce packages of Poppers Mozzarella Cheese Sticks with code numbers as referenced above are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Monogram Foods at 1 (855) 556-1351 Monday – Friday 8am – 5pm CST.
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Expanded #foodsafety #recall of additional 1,650 lbs of Frozen Swai Fillets distributed without meeting import requirements

U.S. Cado Holdings, Inc. Recalls Imported Siluriformes Fish Products Distributed Without Meeting Fsis Requirements

Class I Recall052-2016 EXP-2
Health Risk: HighJul 14, 2016
Congressional and Public Affairs 
Nina A. Anand
(202) 720-9113
Press@fsis.usda.gov
EDITORS NOTE: This release is being reissued as an expansion of the June 20, 2016  and June 25, 2016 recalls to include additional products, production dates, and distribution area. The first recall 052-2016 on June 20, 2016 involved 25,760 pounds of frozen swai fillet products. The recall expansion on June 25, 2016 involved an additional 2,235 pounds of Individually Quick Frozen (IQF) Swai fillet products. The second recall expansion on July 14, 2016  involved an additional 1,650 pounds of frozen Swai Fillets. The combined number of recalled product from June 20, 2016 to July 14, 2016 is 29,645 pounds of frozen Swai imported from Vietnam.
WASHINGTON, July 14, 2016 – U.S. Cado Holdings, Inc., a Santa Ana, Calif. establishment, is recalling approximately 1,650 pounds of imported, frozen Swai fillets products that were distributed into U.S. commerce without meeting federal importation requirements, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The Deep Water Sea Food brand Frozen Swai fillets were produced on April 5, 2016. The following products are subject to recall:
  • 15-lb. boxes containing bulk pieces of “Frozen Swai Fillets” with the label DEEP WATER SEA FOOD, “Production Date: 04/05/2016,” and “Best Before Date: 10/05/2017.” The products subject to recall bear the Factory Number UCH001 on the box and bear the lot number 1683475. These items were shipped to institutional locations in Puerto Rico. The boxes are marked as “9/11 oz.”
The problem was discovered when the customer and import establishment notified FSIS personnel of Swai products entering U.S. commerce without meeting FSIS regulatory requirements for imported Siluriformes. The products were imported from Vietnam and failed to comply with FSIS requirements concerning residue sampling and testing prior to entry into United States commerce. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
Details of the first expansion are: June 25, 2016— U.S. Cado Holdings, Inc., a Santa Ana, Calif. establishment recalled approximately 2,235 pounds of imported, frozen Swai fillets produced and packed on March 1, 9, and 16, 2016 in Vietnam by Golden Quality Seafood Corporation. The following products are subject to recall:
  • 15-lb. boxes containing individually wrapped pieces of “Skinless and Boneless Swai Fillets” with the label DELTA’S BEST BASA BRAND and the lot number 023015 and 023021, and best by dates of 03-01-2018, 03-09-2018, and 03-16-2018.
The products subject to recall bear no plant number on the box, but do bear the lot number 023015 and 023021, and best by dates of 03-01-2018, 03-09-2018, and 03-16-2018. These items were shipped to retail locations in Louisiana, Mississippi, and Texas.
The problem was discovered when the customer and imported establishment notified FSIS personnel of Swai products entering U.S. commerce without meeting FSIS regulatory requirements for imported Siluriformes. The products were imported from Vietnam and failed to comply with FSIS requirements concerning residue sampling and testing prior to entry into United States commerce. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
Details of the first recall are: June 20, 2016– U.S. Cado Holdings, Inc., a Santa Ana, Calif. establishment, recalled approximately 25,760 pounds of imported, frozen Swai fillets products that were distributed into U.S. commerce without meeting federal requirements.
The skinless and boneless Sea Queen brand Swai Fillet items were produced and packed on March 30, 2016, in Vietnam by Golden Quality Seafood Corporation. The following products are subject to recall:         
  • 2-lb. (32-oz.) packages containing individually wrapped pieces of “Skinless and Boneless Swai Fillets.”
The products subject to recall bear plant number FN1158, lot number SW1601-02-16090, and have a “best by” date of March 30, 2018. These items were shipped to Aldi distribution centers in Connecticut, Georgia, Maryland, Pennsylvania, and Tennessee.
The problem was discovered when the customer and import establishment notified FSIS personnel of Swai products entering U.S. commerce without meeting FSIS regulatory requirements for imported Siluriformes. The products were imported from Vietnam and failed to comply with FSIS requirements concerning residue sampling and testing prior to entry into United States commerce. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction 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. Consumers and Media with questions about the recall can contact Paul Nguyen, U.S. Cado Holdings Inc., Manager, at (714) 973-2272.
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 at www.fsis.usda.gov/recalls.
 Under the Federal Meat Inspection Act and implementing regulations, the Food Safety and Inspection Service (FSIS) ensures that Siluriformes fish and fish products in foreign and domestic commerce are safe, wholesome, and not adulterated or misbranded. FSIS samples imported product for drug, pesticide, and other chemical residues. For more information, please visit:http://www.fsis.usda.gov/wps/portal/fsis/topics/inspection/siluriformes/operations-inspection under Hold-and-Test Sampling Protocol for Shipments of Siluriformes Fish/Fish Products from Foreign Establishments that Export Product that Contains a Violative Chemical Residue(s) as Identified by FSIS Border Sampling and Testing.

New #foodsafety #recall possible #Ecoli #contamination of Marie Callender’s Cheese Biscuit Mix

International Commissary Corporation Issues Voluntary Recall of Marie Callender’s Cheese Biscuit Mix Due To Possible Health Risk

July 13, 2016

Contact

Consumers

Joanna Fraire
 Joanna@commissary.com
 408-792-3123

Media

Joanna Fraire
 Joanna@commissary.com
 408-792-3123

Announcement

San Jose, CA. – International Commissary Corporation (ICC) has issued a voluntary recall of certain lots of two retail products: Marie Callender’s 7oz & 14oz Cheese Biscuit Mix. The 7 oz recalled product has Best By dates of 3/22/17 and 5/17/17 and was sold in retail stores in the following states – AL, CA, WA, UT, and TX. The 14 oz recalled product has a Best Buy date of 6/17/17 and was sold only in Stockton, CA.
Most strains of E. coli are harmless, however, others can make you sick. E. coliO121 is a potentially deadly bacterium that can cause bloody diarrhea and dehydration. People who experience these symptoms should seek emergency medical care immediately. The very young, seniors, and those with compromised immune systems are the most susceptible to food borne illness. Anyone diagnosed by a physician as having an illness related to E. coli O121 should contact state and local public health authorities.
ICC was notified by a supplier that an ingredient contains flour which was recalled by General Mills because it may be contaminated with E. coli O121. No other Marie Callender Cheese Biscuit Mix Best By dates are affected. Food Safety is our highest priority and we have taken this action out of an abundance of caution, to protect public health. We are unaware of any illnesses to date from the recalled Marie Callender Cheese Biscuit Mix products.
Consumers who have purchased any of the recalled products are urged to throw them away. Retailers who received the recalled products are being contacted. FDA and the Centers for Disease Control (CDC) warn that consumers should refrain from consuming any raw products made with flour. This recall is being made with the knowledge of FDA.
“The quality of Marie Callender’s products and the safety of our customers are the upmost important issues said Kevin Greene, VP of Sales At ICC, we care deeply about people, our consumers, our employees and our supplier partners. We are working with our retail customers and the FDA to ensure any affected product is removed from the marketplace immediately. We thank you for your patience, and appreciate your continued trust that we will do the right thing for our consumers. Consumers and media with questions can contact Joanna Fraire at 408-792-3123, Monday through Friday, from 9 AM to 4 PM Pacific or at Joanna@commissary.com
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New #foodsafety #recall #undeclared #egg and #soy #allergen in 4,225 pounds of Michael Angelo’s Shrimp Scampi products

Michael Angelo’s Gourmet Foods, Inc. Recalls Shrimp Scampi Products Due To Misbranding and Undeclared Allergens

Class I Recall059-2016
Health Risk: HighJul 13, 2016
Congressional and Public Affairs 
Sarah R. Lichtman
(202) 720-9113
Press@fsis.usda.gov
WASHINGTON, July 13, 2016 – Michael Angelo’s Gourmet Foods, Inc., an Austin, Texas establishment, is recalling approximately 4,225 pounds of frozen shrimp scampi products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products may be mislabeled and contain chicken, as well as egg and soy, known allergens, which are not declared on the product label. 
The following products are subject to recall: [View Label (PDF Only)]
  • 26-oz. boxes, containing plastic trays, labeled, “Michael Angelo’s Uncompromisingly Italian-Style Shrimp Scampi with Linguini Pasta in a Fresh Heirloom Garlic-Butter Sauce” with a packaging date of May 7, 2016, “BEST IF USED BY” date of May 7, 2017 and UPC code 0 37363 98377 0.
Due to a packaging error, products are labeled as, “Michael Angelo’s Uncompromisingly Italian-Style Shrimp Scampi with Linguini Pasta in a Fresh Heirloom Garlic-Butter Sauce;” however, the packages may contain a chicken piccata product, which contains chicken, egg and soy, ingredients not declared on the label. The products subject to recall do not bear the USDA mark of inspection, as shrimp products are regulated by the U.S. Food and Drug Administration (FDA). These items were shipped to distributors in the Southeastern U.S.
The problem was discovered after the firm received a customer complaint.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury, illness or allergic reaction 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 at www.fsis.usda.gov/recalls.
Consumers with questions about the recall can contact the firm’s consumer hotline, at 1 (877) 482-5426. Media with questions about the recall can contact Richard Price, Vice President of Operations, Michael Angelo’s Gourmet Foods, Inc., at (512) 218-3514.

IKEA expanded #foodsafety #recall #undeclared #milk, #almond, and/or #Hazelnuts on certain Chocolate Products

IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products

July 6, 2016

Contact

Consumers

www.IKEA-usa.com
1-888-966-4532

Announcement

CHOKLAND MÖRK, CHOKLAND MÖRK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NÖT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. “All Best Before Dates,” Sold from April 30, 2015 to July 1, 2016.
IKEA had samples of chocolate analyzed and found them to contain milk, hazelnut and/or almond. Persons allergic to milk, hazelnuts and/or almonds may have a severe to life-threatening reaction after consuming the dark chocolate.
Products have been distributed Nationwide at IKEA retail stores and sold individually. There has been no complaints or reported incidents in the United States to date. IKEA of Sweden has had one reported complaint in Japan. The chocolate products do carry an advisory statement, which identifies that the chocolate products may contain milk and tree nuts.
Consumers are encouraged to return the affected products to the nearest IKEA store for a full refund, proof of purchase is not required. If you have any questions or concerns please call Customer Service toll free (24/7) at 1-888-966-4532 orwww.IKEA-usa.com.
We are sorry for any inconvenience this may cause.
IKEA recalls
Product Name Size UPC Undeclared Allergens
CHOKLAD MORK Dark Chocolate Bar 3.5 oz. (100g) 1002939270003 Milk, Almond, Hazelnut
CHOKLAD MORK 70% Dark Chocolate Bars 3.5 0z. (100g) 1203080940009 Milk, Almond, Hazelnut
CHOKLAD LINGON & BLABAR 6.3 0z (180g) 1602184210009 Hazelnut, Almond
GODIS CHOKLADKROKANT Milk chocolate with butterscotch 15.9 oz. (450g) 1202155040002 Hazelnut, Almond
GODIS CHOKLADRAN Wafer filled and covered with chocolate 5.9 oz. (168g) 1202290300009 Hazelnut, Almond
CHOKLAD LJUS Milk Chocolate Bar 3.5 oz. (100g) 1402939250003 Hazelnut, Almond
CHOKLAD NÖT Milk Chocolate with hazelnut 3.5 oz. (100g) 1202939260008 Almond
 
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New #foodsafety #recall possible #Ecoli #contamination of Kerry Inc., Golden Dipt® Jalapeño Breaders

Kerry Inc. Recalls Golden Dipt® Jalapeño Breaders Because of Possible Health Risk

July 12, 2016

Contact

Consumers

Kerry, Inc.
 1-800-325-3383

Media

Jim Egan
 608-299-5100

Announcement

Kerry Inc. of Beloit, WI is recalling two lots of Golden Dipt® Jalapeño Breader that were sold to foodservice distributors because one of our suppliers recalled an ingredient used in our mix for the potential presence of E. coli O121. Kerry Inc. was notified by our supplier that two of their products, a red bell pepper nugget and a jalapeno nugget, were made with a small percentage of affected flour which was recalled by General Mills because it may be contaminated with E. coli O121.
Most strains of E. coli are harmless, however, others can make you sick. E. coliO121 is a potentially deadly bacterium that can cause bloody diarrhea and dehydration. People who experience these symptoms should seek emergency medical care immediately. The very young, seniors, and those with compromised immune systems are the most susceptible to foodborne illness. Anyone diagnosed by a physician as having an illness related to E. coli 0121 should contact state and local public health authorities.
No illnesses have been reported to date with the Kerry Inc. products. No other Kerry Inc. products are affected by this recall.
These two lot codes of Golden Dipt® Jalapeño Breader were manufactured by Kerry Inc. and sold to foodservice distributors located in Florida, Texas, Oklahoma, Illinois, Minnesota, New Jersey, Missouri and regions of Canada. Product may have been further distributed beyond these locations throughout the foodservice industry and to retail stores open to the general public.
The affected Golden Dipt® Jalapeño Breader is in a white 10 pound bag with the UPC number 763089721548 and Item Number: G5620.690. The recall only affects lots 0414647003 and 0513647003. The lot code is printed along the bottom of the label, as illustrated below.
If you have purchased Golden Dipt® Jalapeno Breader with either of the lot codes noted above, please dispose of the product and seek reimbursement with the distribution group/store where it was purchased. Questions can be directed to Kerry 800-325-3383 between the hours of 8 am to 5 pm CST.
This recall is being made with the knowledge of the U.S. Food and Drug Administration.
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New #foodsafety #recall #undeclared #milk #allergen in Snack Factory® Original Pretzel Crisps®

Baptista’s Bakery Issues Allergy Alert on Undeclared Milk in Snack Factory® Original Pretzel Crisps®

July 12, 2016

Contact

Consumers

Snack Factory® Consumer Affairs
 info@pretzelcrisps.com
 1-888-683-5400

Media

Laura Villarreal
 414-409-2123

Announcement

Baptista’s Bakery, Inc. announced a voluntary recall of a limited number of 30 oz. Snack Factory® Original Pretzel Crisps® packages because they may contain undeclared milk ingredients. People who have an allergy or severe sensitivity to milk run the risk of a serious or life threatening allergic reaction if they consume the affected product.
This voluntary recall covers only the following product:
Snack Factory® Original Pretzel Crisps® 
30 oz packages
UPC code: 049508250401 
Best By Date: 07-01-17
No other Snack Factory® Original Pretzel Crisps® products or sizes were impacted.
We are initiating this recall out of an abundance of caution after determining that seasoned product produced in the same facility may have been commingled with the product listed above.
No illnesses have been reported as a result of this issue. Baptista’s Bakery has informed the U.S. Food & Drug Administration of this voluntary recall.
To locate the Best By date, consumers should look on the bottom of the package. Consumers who have purchased the product listed above should not consume it, but should dispose of it or return it to the store where it was originally purchased. Consumers may also contact Snack Factory® Consumer Affairs for a full refund online at info@pretzelcrisps.com or by calling (888) 683-5400 between 8am and 5pm Central Standard Time. Please direct additional questions or concerns to Laura Villarreal at 414-409-2123 between 8 am and 6pm Central Standard Time.
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Additional #foodsafety #recall possible #Ecoli #flour #contamination of two flavor Betty Crocker Cake Mix

Two Flavors of Betty Crocker Cake Mix Recalled

July 11, 2016

Contact

Consumers

General Mills
 800-230-8103 (U.S.)
 800-526-4579 (Canada)

Media

General Mills Corporate Communications
 Media.line@genmills.com
 763-764-6364

Announcement

Consumers reminded not to consume uncooked cake batter or raw flour products
MINNEAPOLIS – Out of an abundance of caution, two flavors of Betty Crocker cake mix sold in the U.S. and one flavor sold in Canada have been added to General Mills’ previously announced flour recall from July 1, 2016. No illnesses reported to date have been connected to cake mix. No other General Mills or Betty Crocker mixes are included in this recall.
Two flavors of cake mix — Betty Crocker Delights Super Moist Party Rainbow Chip Cake Mix (called Betty Crocker Super Moist Rainbow Bit Cake Mix in Canada) and Betty Crocker Delights Super Moist Carrot Cake Mix — have been added to the recall as they contain flavor chips (or bits) produced using Wondra flour, which was included in General Mills’ previous July 1st recall announcement. General Mills continues to collaborate with health officials to investigate a multistate outbreak ofE. coli O121 connected to several brands of flour.
This recall applies only to the specific product and date codes listed below.
The affected Betty Crocker cake mixes sold in the U.S.:
Betty Crocker Delights Super Moist Party Rainbow Chip Cake Mix
Package UPC 000-16000-40997
Recalled Better if Used by Dates 25MAR2017, 28MAR2017, 27APR2017, 28APR2017, 23MAY2017, 24MAY2017, 25MAY2017
Betty Crocker Delights Super Moist Carrot Cake Mix
Package UPC 000-16000-40987
Recalled Better if Used by Dates 12APR2017, 13APR2017, 14APR2017, 28MAY2017, 29MAY2017, 30MAY2017, 07JUL2017, 08JUL2017
The affected Betty Crocker cake mix sold in Canada:
Betty Crocker Super Moist Rainbow Bit Cake Mix
Package UPC 000-65633-46589
Recalled Better if Used by Dates 27AL2017, 08JN2017, 09JN2017
If you possess any products included in this recall, they should be thrown away. A full list of retail products included in the flour recall can be found athttp://www.generalmills.com/flourdisclaimer icon.
Guidance from the Food and Drug Administration (FDA) and the Centers for Disease Control (CDC) continues to be that consumers should refrain from consuming any raw dough or batter products. E. coli O121 is eliminated by heat through baking, frying, sautéing or boiling products. All surfaces, hands and utensils should be properly cleaned after contact with flour, batter, or dough.
Although most strains of E. coli are harmless, others can make you sick. E. coliO121 is a potentially deadly bacterium that can cause bloody diarrhea and dehydration. Seniors, the very young, and persons with compromised immune systems are the most susceptible to foodborne illness.
Anyone diagnosed by a physician as having an illness related to E. coli O121 is also urged to contact state and local public health authorities.
U.S. consumers with questions or requesting Betty Crocker replacement product should contact General Mills at 800-230-8103. Canadian consumers with questions about the Betty Crocker products including in the recall, or requesting replacement, should contact General Mills Canada at 800-526-4579. Additional recall information can also be found at http://www.generalmills.com/flourdisclaimer icon.
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