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Found 31 results

  1. http://www.fda.gov/Safety/Recalls/ucm531882.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery John
  2. http://www.fda.gov/Safety/Recalls/ucm531359.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery John
  3. http://www.fda.gov/Safety/Recalls/ucm530639.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery John
  4. http://www.fda.gov/Safety/Recalls/ucm530398.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Sabra Dipping Company’s Recall Prompts Secondary Recall of Vegetable Products For Immediate Release November 21, 2016 Contact Consumers Taylor Farms 855-455-0098 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm530398.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos Following the Sabra Dipping Co., LLC’s ("Sabra’s") recall where select Sabra's products were recalled due to the potential of being contaminated with Listeria monocytogenes, Taylor Farms Tennessee, Inc., Taylor Farms Texas, Inc. and Taylor Farms Pacific, Inc. (all collectively referred to as “Taylor Farms”) are voluntarily recalling a limited number of products that contain Sabra's recalled products. The recalled products are labeled “Taylor Farms Veggie and Hummus Bistro Boxes” and “Schnucks Vegetable and Hummus Snack Trays” containing Sabra Hummus Classic 2 oz. dipping cups. The Taylor Farms products subject to the recall are limited to the code dates provided. No other Taylor Farms products are impacted by this recall. Product Description UPC Use By Dates Taylor Farms Veggie & Hummus Bistro Box 0 30223 01037 1 11/11/16 – 12/1/16 Schnucks Vegetable and Hummus Snack Tray 0 41318 09193 9 11/18/16 & 11/23/16 (Please refer to Sabra’s recall notice for details regarding individual Sabra items and lot codes/”Best Before” dates, also located on the lid or bottom of the dipping cups.) These products are being recalled because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. Taylor Farms has not received any reports of illnesses associated with these recalled items. The recalled products were distributed from October 30, 2016 – November 18, 2016. The grocers involved have been instructed to remove any remaining product from their shelves and to dispose of any of the remaining product in their inventory. The recalled products were distributed in Arkansas, California, the District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maryland, Michigan, Missouri, North Carolina, Nevada, Oklahoma, Oregon, South Carolina, Tennessee, Texas, Virginia, Wisconsin, and West Virginia. Customers who have purchased these products are urged not to consume the products and should dispose of the recalled products immediately. Consumers may call for further information at (855) 455-0098 between the hours of 9 am (PST) and 5 pm (PST) Monday through Friday. Consumers with concerns about an illness from consumption of this product should contact a health care provider. John
  5. http://www.fda.gov/Safety/Recalls/ucm529000.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Free2b Foods Issues Allergy Alert on Undeclared Milk Ingredient in Chocolate Sun Cups For Immediate Release November 10, 2016 Contact Consumers David Lurie hey@free2bfoods.com 844-610-5673 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm529000.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos November 11, 2016 – Boulder, CO - Free2b Foods of Boulder, CO is recalling its chocolate Sun Cups for three specific Sell By dates, because it may contain undeclared milk ingredients. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products. The recalled chocolate Sun Cups were distributed nationwide in retail stores. Specifics on the recalled products are found below. UPC codes are printed on the back of packages and Sell By dates are stamped in black on the back of packages. Product Name Package UPC Code Sell By Dates Chocolate Sun Cups Double cups in purple package 895444001405 02 Aug 17 04 Aug 17 07 Aug 17 Chocolate Sun Cups Single cups in purple package 895444001443 02 Aug 17 04 Aug 17 07 Aug 17 The issue was discovered as a result of a consumer communication. One reaction has been reported to the company to date. Subsequent investigation by the company indicates that this milk-containing product was distributed in packaging that did not reveal the presence of milk. This occurred during a transition the company recently made to remove dairy from its products and facility while moving from a top 7 Allergen-Free facility to a Top 8 Allergen-Free facility. They are now a dedicated Top 8 Allergen-Free manufacturing facility. If you have these Sun Cups and a milk allergy, do not consume them. Please photograph the package with UPC code, then dispose of them or return them to: Free2b Foods, 5305 Spine Road #E Boulder, CO 80301. Free2b Foods will reimburse or replace products with new chocolate Sun Cups. For questions, please contact 844-610-5673 between 8am-10pm MST or email hey@free2bfoods.com. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. About Free2b Foods: Based in Boulder, CO, Free2b Foods helps families with food allergies and others with snacking solutions free from top allergens. The company first introduced their popular Sun Cups in 2008 in response to a father’s plea to make a chocolate cup that was safe for his peanut allergic son. The company has been serving families with food allergies and sensitivities faithfully since it opened its doors with products that were free from 7 of the Top 8 allergens. The company recently removed dairy from its recipes and manufacturing plant, and as of September 2016, Free2b Foods has a dedicated facility that is Top 8 Allergen-Free. The team is just as passionate about taste as they are about quality and safety. Sourcing highest quality ingredients, their treats are made in small batches. In addition to making a variety of gourmet chocolate cups, they recently launched a line of Top 8 Allergen-Free chocolate bars. Free2b is available in retailers nationwide. John
  6. http://www.fda.gov/Safety/Recalls/ucm528731.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. ISB Food Group, LLC Recalls L.A. Creamery Honeycomb Ice Cream And L.A. Creamery Salted Caramel Ice Cream With Expiration Dates Of March 18, 2017 Because Of Possible Health Risk For Immediate Release November 9, 2016 Contact Consumers Antonella Loiacano 818-405-0022, ext. 103 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm528731.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos Los Angeles, CA - ISB Food Group, LLC is recalling L.A. Creamery Honeycomb ice cream and L.A. Creamery Salted Caramel ice cream with expiration dates of March 18, 2017, because they were produced in a co-packing facility that has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. L.A. Creamery Honeycomb and L.A. Creamery Salted Caramel with expiration dates of March 18, 2017, were distributed from March to October 2016 in California, New York, New Jersey, Connecticut, Florida, Pennsylvania, Maryland and Massachusetts. The product is in paper 14 oz. ice cream containers with the L.A. Creamery brand name, Salted Caramel flavor and Honeycomb flavors, specifically stamped on the bottom of the container with the expiration date of March 18, 2017. No illnesses have been reported to date, and no L.A. Creamery product has been found to be contaminated. The recall is the result of the U.S. Food and Drug Administration (FDA) finding samples positive for Listeria monocytogenes in the facility of the contract manufacturer, Dr. Bob’s of Upland, LLC, and in finished product of an unrelated company’s brand that was manufactured at the Dr. Bob’s facility, leading the contract manufacturer to recall all ice cream products produced this year at its facility. The continuous production line at Dr. Bob’s that tested positive for Listeria monocytogenes was used to produce L.A. Creamery Salted Caramel and L.A. Creamery Honeycomb flavors in March of 2016. ISB Food Group has only used the Dr. Bob’s facility for co-packing once in 2016, in March, and will not produce in the Dr. Bob’s facility going forward. Consumers who have purchased L.A. Creamery Salted Caramel flavor or L.A. Creamery Honeycomb flavor with expiration dates of March 18, 2017 are urged to contact us for a full refund or any questions at (818) 405-0022, extension 103, Monday through Friday, 7:00 am Pacific Time to 3:00 pm Pacific Time. John
  7. http://www.fda.gov/Safety/Recalls/ucm528730.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. ISB Food Group, LLC Recalls Nancy’s Fancy Butterscotch Budino Gelato And Nancy’s Fancy Peanut Butter With Crunchy Peanuts Gelato With Expiration Dates Of March 18, 2017 Because Of Possible Health Risk For Immediate Release November 9, 2016 Contact Consumers Antonella Loiacano (818) 405-0022, ext. 103 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm528730.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos ISB Food Group, LLC of Los Angeles, California is recalling Nancy’s Fancy Butterscotch Budino Gelato and Nancy’s Fancy Peanut Butter with Crunchy Peanuts Gelato with expiration dates of March 18, 2017, because they were produced in a co-packing facility that has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. Nancy’s Fancy Butterscotch Budino Gelato and Nancy’s Fancy Peanut Butter with Crunchy Peanuts Gelato with expiration dates of March 18, 2017, were distributed from March to October 2016 in California, Oregon and Texas. The product is in plastic pint-sized containers with the Nancy’s Fancy brand name, Butterscotch Budino flavor and Peanut Butter with Crunchy Peanuts flavor, specifically stamped on the bottom with the expiration date of March 18, 2017. No illnesses have been reported to date, and no Nancy’s Fancy product has been found to be contaminated. The recall is the result of the U.S. Food and Drug Administration (FDA) finding samples positive for Listeria monocytogenes in the facility of the contract manufacturer, Dr. Bob’s of Upland, LLC, and in finished product of an unrelated company’s brand that was manufactured at the Dr. Bob’s facility, leading the contract manufacturer to recall all ice cream products produced this year at its facility. The continuous production line at Dr. Bob’s that tested positive for Listeria monocytogenes was used to produce Nancy’s Fancy Butterscotch Budino and Peanut Butter with Crunchy Peanuts flavors in March of 2016. ISB Food Group has only used the Dr. Bob’s facility for co-packing once in 2016, in March, and will not produce in the Dr. Bob’s facility going forward. Consumers who have purchased Nancy’s Fancy Butterscotch Budino flavor or Nancy’s Fancy Peanut Butter with Crunchy Peanuts flavor with expiration dates of March 18, 2017 are urged to contact us for a full refund or any questions at (818) 405-0022, extension 103, Monday through Friday, 7:00 am Pacific Time to 3:00 pm Pacific Time. John
  8. http://www.fda.gov/Safety/Recalls/ucm527207.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Mondelēz Global LLC Conducts Nationwide Voluntary - Recall of Oreo Fudge Cremes Product Sold in the U.S. Recall Due to Milk Allergen Not Listed in Ingredient Line For Immediate Release October 28, 2016 Contact Consumers Consumer Relations 1-855-535-5948 Media Laurie Guzzinati news@mdlz.com +1-847-943-5678 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm527207.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos East Hanover, N.J. – Mondelez Global LLC announced today a nationwide voluntary recall in the United States, including the U.S. Territories of Puerto Rico, St. Croix and St. Thomas, of certain Oreo Fudge Cremes product, Original and Mint varieties, due to milk allergen not being declared in the ingredient list. Mondelez Global LLC is taking this action out of an abundance of caution. Consumers may be informed about the potential presence of milk by an allergen advisory statement already included on the label (“Manufactured on equipment that processes milk....”). People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product. The following product is being recalled: Description Retail UPC Best When Used By Dates Oreo Fudge Cremes, Original variety (11.3 oz package) 0 44000 02694 3 19 AUG 16 20 AUG 16 14 SEP 16 13 OCT 16 14 OCT 16 17 OCT 16 (see code date on bottom left corner on back of package) Oreo Fudge Cremes, Mint variety (11.3 oz. package) 0 44000 02696 7 20 AUG 16 21 AUG 16 14 SEP 16 15 SEP 16 16 SEP 16 17 OCT 16 18 OCT 16 (see code date on bottom left corner on back of package) This recall is limited exclusively to this Oreo Fudge Cremes product, Original and Mint varieties, sold in the U.S., including the U.S. Territories of Puerto Rico, St. Croix and St. Thomas, and no other products are included in this recall. To date, one report of an allergic reaction has been received related to the above-listed “Best When Used By” dates. This recall is a result of analysis conducted by the FDA related to this product. Consumers who have this product should not eat it and should discard any products they may have. Consumers can contact the company at 1-855-535-5948, 24 hours a day to get more information about the recall, and Consumer Relations specialists are available Monday – Friday, 9 a.m. to 6 p.m. ET. John
  9. http://www.fda.gov/Safety/Recalls/ucm518666.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Snyder’s-Lance Issues Voluntary Recall of 4oz Diamond of California® Chopped Macadamia Nuts and 2.25oz Diamond of California® Macadamia Halves & Pieces Because of Possible Health Risk For Immediate Release August 30, 2016 Contact Consumers Consumer Affairs http://diamondfoods.com/contact/ 503-364-0399 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm518666.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos Snyder’s-Lance, Inc. is initiating a voluntary recall of Diamond of California® Macadamia Nuts, distributed in retail stores nationwide, due to possible Salmonella contamination. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. There have been no reported illnesses to date. This voluntary recall is the result of testing by a FDA-contracted laboratory which revealed that a 4oz package of Diamond of California® Chopped Macadamia Nuts contained Salmonella. This voluntary recall covers only the following products: 4oz Diamond of California® Chopped Macadamia Nuts 2.25oz Diamond of California® Macadamia Halves and Pieces The voluntary recall is limited to multiple production codes of the two products listed below. To locate the production code on the package, consumers should look on the front of the package. No other production codes, sizes or varieties of Diamond of California® products are affected by this recall. Product Name UPC Code Lot Number Best Before Date Diamond of California® Chopped Macadamia Nuts, 4oz 010300345848 16137D331S 16138D331S 16158D331S 16 NOV 2017 17 NOV 2017 06 DEC 2017 Diamond of California® Macadamia Halves & Pieces, 2.25oz 070450743918 16137D331S 16159D331S 16 NOV 2017 07 DEC 2017 Consumers who may have purchased the product listed above should not consume it but should contact Consumer Affairs for a full refund online at http://diamondfoods.com/contact/ or by calling 503-364-0399 between 8am and 5pm Pacific Time, Monday – Friday. The quality and safety of our products is the top priority for our company. We apologize to our retail customers and consumers and sincerely regret any inconvenience. We are working and cooperating fully with the U. S. Food & Drug Administration on this voluntary recall. John
  10. http://www.fda.gov/Safety/Recalls/ucm517720.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Baptista’s Bakery Issues Allergy Alert on Undeclared Milk in Snack Factory® Original Pretzel Crisps® For Immediate Release August 17, 2016 Contact Consumers Snack Factory® Consumer Affairs info@pretzelcrisps.com (888) 683-5400 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm517720.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos Baptista’s Bakery, Inc. announced a voluntary recall of a limited number of 7.2 oz. Snack Factory® Original Pretzel Crisps® and 7.2 oz Snack Factory® Sriracha Lime 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 the following products: Snack Factory® Original Pretzel Crisps® 7.2 oz packages UPC code: 049508006008 Best By Date: 07-01-17 Snack Factory® Sriracha Lime Pretzel Crisps® 7.2 oz packages UPC code: 049508006060 Best By Date: 07-01-17 No other Snack Factory® Original Pretzel Crisps® or Snack Factory® Sriracha Lime 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. John
  11. http://www.fda.gov/Safety/Recalls/ucm510899.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Two Flavors of Betty Crocker Cake Mix Recalled For Immediate Release 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 View Product Photos http://www.fda.gov/Safety/Recalls/ucm510899.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos 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 of E. 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 at http://www.generalmills.com/flour. 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. coli O121 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/flour. Previous Release http://www.fda.gov/Safety/Recalls/ucm509693.htm FDA Investigates Multistate Outbreak of E. coli O121 Infections Linked to Flour http://www.fda.gov/Food/RecallsOutbreaksEmergencies/Outbreaks/ucm504192.htm John
  12. http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2016/recall-056-2016-release News Release ConAgra Foods Recalls Frozen Chicken and Beef Products Due to Possible Foreign Matter Contamination Class I Recall 056-2016 Health Risk: High Jul 6, 2016 Congressional and Public Affairs Veronika Medina (202) 720-9113 Press@fsis.usda.gov WASHINGTON, July 6, 2016 – ConAgra Foods, a Russellville, Ark. establishment, is recalling approximately 3,806 pounds of frozen chicken and beef entrée products that may be contaminated with extraneous materials, specifically metal, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The metal fragments range in size between 2 and 9 millimeters (mm) in diameter, and are curled, malleable and shiny. The metal fragments may be embedded in the sauce contained within the frozen entrée products. The frozen chicken and beef entrée items were produced on June 13, 2016 and June 22, 2016. The following products are subject to recall: View Labels PDF only http://www.fsis.usda.gov/wps/wcm/connect/ed8b9d45-e972-4236-a75e-81ae7165acd0/056-2016-label.pdf?MOD=AJPERES 22-oz. plastic bagged meal packages of “P.F. Chang’s Home Menu Brand Signature Spicy Chicken.” with “Use By” date of 6/08/17 and case code 5006616500. 22-oz. plastic bagged meal packages of “P.F. Chang’s Home Menu Brand Mongolian Style Beef.” with “Use By” date of 6/17/17 and case code 5006617400. The products subject to recall bear establishment number “EST. 233” inside the USDA mark of inspection. These items were shipped to distributors and retail locations in Arkansas, Illinois, Michigan, Minnesota, New York, Vermont, and Wisconsin. The problem was discovered July 1, 2016, when an establishment employee observed metal fragments while dispensing sugar from a supplier for sauce formulation during processing. The resulting sauce is a component in the frozen entrée products. There have been no confirmed reports of adverse reactions or injuries 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 1-800-252-0634. Members of the media with questions about the recall can contact Kristine Mulford, Manager of Communications, at (312) 549-5522. John
  13. http://www.fda.gov/Safety/Recalls/ucm508786.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. IKEA N.A. Services, LLC Issues Allergy Alert on Undeclared Milk, Almond, Hazelnut in the CHOKLAD MORK and CHOKLAD MORK 70% Dark Chocolate Bars, Net Wt. 3.5 oz. For Immediate Release June 24, 2016 Contact Consumers Customer Service 1-888-966-4532 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm508786.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos IKEA recalls CHOKLAD MÖRK UPC Code 100293927003 and CHOKLAD MÖRK 70% UPC Code 1203080940009 Dark Chocolate Bars, Net Wt. 3.5 oz. are being recalled due to undeclared Milk, Hazelnuts and Almonds. All Best Before Dates Of CHOKLAND MÖRK and CHOKLAND MÖRK 70% are being recalled due to undeclared Milk, Hazelnuts and Almond. IKEA had samples of the dark chocolate bars analyzed and found them to contain milk, hazelnut and 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 dark chocolate bars do carry an advisory statement, which identifies that the dark chocolate 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 or www.IKEA-usa.com. We are sorry for any inconvenience this may cause. John
  14. http://www.fda.gov/Safety/Recalls/ucm508590.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Figi's Issues Recall Alert Due To Possible Health Risk For Immediate Release June 24, 2016 Contact Consumers Figi's Companies, Inc. 1-800-437-3817 Media Sheri Dick 715-384-1462 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm508590.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos Figi's Companies, Inc of Marshfield, WI is recalling the following 2 products that are related to the SunOpta sunflower kernel recall, because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. 16 oz. Snack Shoppe Hot & Spicy Cajun Snack Mix in a foil bag that is contained in a tin box. The foil bags are marked with lot HD116063 160ZHSMIX. 16 oz Figi's Nature's Mix in a plastic bag that is in a red circular tin container. Nature's Mix is packaged in a plastic bulk bag with approximately 8-12 ounces of product. There is no lot information on the bag. The recalled Hot & Spicy Cajun Snack Mix was distributed nationwide through mail orders. The Nature's Mix 16 oz red circular tins were distributed nationwide through a distributor who sold directly to consumers and the Nature's Mix in clear plastic bags were only distributed through Figi's Outlet Store located in Marshfield, WI. No illnesses have been reported to date in connection with this problem. Figi's was notified by our supplier that there is a potential for contamination. The production of the two noted products has been suspended while the source of the problem is being investigated. Production will resume when a suitable resolution is found. Consumers who have purchased 16 ounce packages of the Hot and Spicy Mix with the lot number noted above or the bulk-packaged Nature's Mix from our Outlet Store are urged to return them to Figi's for a full refund. Consumers with questions may contact Figi's Companies, Inc. Monday - Saturday, 7am - 530pm CST at 1-800-437-3817. John
  15. http://www.fda.gov/Safety/Recalls/ucm508001.htm Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Pinnacle Foods Inc. Voluntarily Recalls Limited Quantity of C&W Early Harvest Petite Peas and C&W Petite Peas Due to Possible Listeria Contamination For Immediate Release June 21, 2016 Contact Consumers Pinnacle Foods Consumer Care 1-888-299-7646 Media Elizabeth Rowland Mediainquiries@pinnaclefoods.com (973)541-8620 Announcement Pinnacle Foods Inc. is voluntarily recalling a limited number of C&W Early Harvest Petite Peas and C&W Petite Peas because they may contain Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. The frozen products are being recalled as a precaution with the health and safety of our consumers as our top priority. Pinnacle Foods initiated the recall after the contract packer of the products, National Frozen Foods, notified the Company of the issue. The Food and Drug Administration has been made aware of this recall. No illnesses have been reported to date. The recalled products were distributed nationally and online. All affected distributors and retail customers are being notified and the recalled products are being removed from store shelves. The recalled items can be identified by a “Best by” code printed on the back of the bag. Only the following codes are affected by this recall: C&W Early Harvest Petite UPC 0-70332-00159-4 16 oz. bag Mar-07-18 Mar-17-18 Mar-28-18 Mar-29-18 Peas C&W Petite Peas UPC 0-70332-00158-7 16 oz. bag Mar-23-18 Mar-28-18 Mar-29-18 No other products produced by Pinnacle Foods are affected by this recall. Consumers should not consume these products. Affected product may be returned to the place of purchase for a full refund. Consumers with questions may contact Pinnacle Foods at 1-888-299-7646. John
  16. http://www.fda.gov/Safety/Recalls/ucm507337.htm Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Kashi Company Expands Date Codes of Two Products Related to Previously Announced Recall of Snack Bars and Bear Naked Granola For Immediate Release June 16, 2016 Contact Consumers Kashi Company 1-877-747-2467 Media Name Callie.Bruhn@edelman.com 503-471-6816 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm507337.htm#recall-photos SOLANA BEACH, Calif. – Kashi Company is amending the date codes for Kashi GOLEAN® Honey Pecan Baklava Bars and Bear Naked® Soft Baked Granola, Cinnamon + Sunflower Butter related to its previously announced recall of snack bars and granola that contain ingredients made from sunflower seeds distributed by its supplier, SunOpta, that have the potential to be contaminated with Listeria monocytogenes. This update includes two new "Best If Used Before" dates on Kashi GOLEAN® Honey Pecan Baklava Bars, and one new "Best If Used By" date on Bear Naked® Soft Baked Granola, Cinnamon + Sunflower Butter. The updated information is: Kashi® GOLEAN® Honey Pecan Baklava Bars, 5-count with UPC Code 18627 10474 – "Best If Used Before"dates of Jul21 16; Aug07 16; Sep13 16; Sep22 16; and Oct20 16 Bear Naked® Soft Baked Granola, Cinnamon + Sunflower Butter, 11 oz pouch with UPC Code 84623 10163 – "Best if Used By"dates of Aug 13 2016 to Jan 11 2017 The date codes can be found on the top of the box of the Honey Pecan Baklava Bars, and at the bottom of the pouch of the Bear Naked Granola. This update impacts product sold only in the United States. More information can be found at www.consumeralert.kashi.com. Consumers can call 1-877-747-2467, Monday through Friday, 9 a.m. – 6 p.m. ET. Consumers may also contact us via https://www.kashi.com/contact-us. This update impacts product sold only in the United States. More information can be found at www.consumeralert.kashi.comdisclaimer icon. Consumers can call 1-877-747-2467, Monday through Friday, 9 a.m. – 6 p.m. ET. Consumers may also contact us via https://www.kashi.com/contact-us Original Release http://www.fda.gov/Safety/Recalls/ucm504285.htm Expanded Release http://www.fda.gov/Safety/Recalls/ucm505058.htm John
  17. http://www.fda.gov/Safety/Recalls/ucm506463.htm Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Honey Bunchie, LLC Recalls a Limited Number of Gourmet Honey Bars That Contain SunOpta Sunflower Kernels due to Possible Health Risk For Immediate Release June 13, 2016 Contact Consumers Honey Bunchie, LLC customercare@honeybunchies.com 303-808-3351 Media Edward Payne edward.payne@honeybunchies.com 720-427-6089 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm506463.htm#recall-photos Longmont, CO. — Honey Bunchie, LLC is initiating a voluntary recall of a limited number of Honey Bunchies Gourmet Honey Bars that contain SunOpta sunflower kernels that have the potential of contamination with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. The recalled products were distributed directly from Honey Bunchie, LLC to distributors, retailers and online consumers between 08/05/2015 – 03/15/2016. To date, Honey Bunchie, LLC has not received any reports of illness; however, the company is initiating this voluntary recall in an abundance of caution as part of its commitment to the health and safety of its consumers. Product Name: Honey Bunchies Gourmet Honey Bar Description UPC Code Size Best By Date Individual Bar 8 66192 00010 1 1.9 oz 12/27/2015 – 10/28/2016 Box of 20 Bars 8 66192 00011 8 20 bars, 1.9 oz each 12/27/2015 – 10/28/2016 No other products produced by Honey Bunchie, LLC are affected by this recall. The affected bars were sold nationwide through distributors, retailers and online. Consumers who have purchased affected product are urged not to consume the product and return it to the place of purchase for a full refund. Online customers should contact the company at customercare@honeybunchies.com. Consumers with questions may contact the company at (303) 808-3351. Retailers and wholesale customers should check their inventories and shelves to confirm none of the affected products are present or available for purchase by consumers or in warehouse inventories. Please contact Honey Bunchie at customercare@honeybunchies.com to arrange for disposal or return of the product. This recall is being made with the knowledge of the Food and Drug Administration. John
  18. http://www.fda.gov/Safety/Recalls/ucm506282.htm#recall-photos Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Bounce USA Recalls Apple Cinnamon Protein Punch Energy Balls Because of Possible Health Risk For Immediate Release June 10, 2016 Contact Consumers Bounce USA 855-441-8966 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm506306.htm#recall-photos Bounce USA of Bend, Oregon is voluntary recalling the Bounce Apple Cinnamon Protein Punch Energy Balls (newly named Apple Cinnamon Protein Energy Balls) because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women. This recall was initiated when the supplier, SunOpta, notified us of the sunflower kernels expanded recall due to the possibility that some sunflower kernels may be contaminated with Listeria monocytogenes. We would like to reassure all of our customers that we have not received any news of consumers being affected by illness to date. The following recalled products were distributed nationwide through retail stores and on-line through Amazon.com between November 4, 2015 and June 6, 2016. No other Bounce products are affected: Bounce 1.48 oz. (42g) Apple Cinnamon Protein Punch Energy Balls Product UPC Codes are 852949003723 (individual packs) and 852949003730 (12-unit boxes) Best Before Dates 04SEP16 and 12NOV16 Bounce 42g Apple Cinnamon Protein Energy Balls Best Before Dates: 23 DEC16, 10 JAN17, 22 FEB17, 31MAR17 Product UPC codes are 852949003723 (individual packs) and 852949003730 (12-unit boxes) Customers who have purchased any of the above products are urged not to consume the products and to dispose of them. Any questions can be directed to Bounce USA by emailing feedbackusa@bouncelifestyle.com or by calling 855-441-8966 Monday-Friday, 9am-5pm PST). We apologize for any inconvenience this may have caused. John
  19. http://www.fda.gov/Safety/Recalls/ucm504754.htm Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Additional Quaker Quinoa Granola Bars Recalled as a Result of Expanded Sunflower Kernel Contamination by SunOpta For Immediate Release June 2, 2016 Contact Consumers 800-856-5781 Media Laura Ude Laura.Ude@pepsico.com (312)821-2039 Announcement The Quaker Oats Company, a subsidiary of PepsiCo, Inc., today announced a second voluntary recall of all Quaker® Quinoa Granola Bars, as a result of further sunflower kernel contamination found by ingredient supplier SunOpta. On May 16, 2016, Quaker took the cautionary measure to issue the voluntary recall on a small quantity of their Quinoa Bars that were potentially impacted by sunflower kernels received from SunOpta that were potentially contaminated with Listeria monocytogenes (L.mono). L.mono is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. Since May 16, SunOpta has conducted additional testing on sunflower kernels that extended beyond the original dates of concern provided. That testing is complete and as a result, out of an abundance of caution and care for the consumer, Quaker has made the decision to expand the initial recall. The products were distributed nationwide and the company is now recalling all of the following Quaker Quinoa Granola Bars: 6.1 ounce boxes of Quaker Quinoa Granola Bars Chocolate Nut Medley with UPC code 30000 32241 and Best Before Dates before 11/15/16. 6.1 ounce boxes of Quaker Quinoa Granola Bars Yogurt, Fruit & Nut with UPC 30000 32243 and Best Before Dates before 11/15/16. Pictures of the products are available on www.quakeroats.com Consumers who have purchased this particular product are urged to dispose of or return them to the place of purchase for a full refund. They can also direct any questions to 800-856-5781, Monday – Friday, 8:30 a.m. – 6:00 p.m. (EST), or find more information at www.quakeroats.com At this time there are no other Quaker products involved in this situation. The company is working closely with the Food and Drug Administration (FDA) and SunOpta to further investigate this issue and ensure it has been contained. John
  20. http://www.fda.gov/Safety/Recalls/ucm504003.htm Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Sid Wainer and Son Recalls Domaine de Provence La Cucina Tart Shells and Domaine de Provence Neutral 3" Cone Tart Shells Due to Undeclared Allergens For Immediate Release May 27, 2016 Contact Consumers Sid Wainer & Son 1-800-423-8333, x168 or x119 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm504003.htm#recall-photos Sid Wainer & Son of New Bedford, MA is voluntarily recalling Domaine de Provence La Cucina Tart Shells and Domaine de Provence Neutral 3” Cone Tart Shells due to undeclared allergens. People who have an allergy or severe sensitivity to Tree Nuts, specifically Coconut and Eggs run the risk of a serious or life-threatening allergic reaction if they consume these products. The product is safe for consumption by those who do not have Coconut or Egg allergy. The product is packaged in a brown cardboard box labeled as: Domaine de Provence La Cucina Tart Shells, 252 pieces per box containing undeclared Eggs with UPC 708152149119 Domaine de Provence Neutral 3” Cone Tart Shells, 308 pieces per box containing undeclared Coconut UPC 708152316856 Both tarts were distributed Nationwide to Food service establishments. No illnesses have been reported to date in connection with this problem. The private manufacturer for Sid Wainer and Son discovered an ingredient change that consisted of an allergen that was not declared on the labels. Consumers who have purchased the above mentioned products are urged to return them to the place of purchase or dispose of the products. Consumers with questions may contact the company at 1-800-423-8333 at extension 168 or 119 between the hours of 9:00 am and 5:00 pm. This recall is being initiated with the knowledge of the Food and Drug Administration. John
  21. http://www.fda.gov/Safety/Recalls/ucm502184.htm Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Expanded Recall Period of Certain Sunflower Kernel Products Due to Possible Contamination By Listeria Monocytogenes For Immediate Release May 18, 2016 Contact Consumers Customer Service contactus@sunopta.com 888-886-4428 Media Rob Litt rob.litt@sunopta.com 952-893-7863 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm499204.htm#recall-photos TORONTO – As a precaution, SunOpta expanded its voluntary recall of a limited number of sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women. The initial recall was limited to sunflower kernel products produced at SunOpta’s Crookston, Minn. facility between the dates of February 1, 2016 and February 19, 2016. The expanded recall includes products produced February 20, 2016 through April 21, 2016, the date on which the facility ceased production of the products. No illnesses have been confirmed related to the consumption of this product. Recalled retail items were sold in clear printed plastic packages and are marked with Best By Dates located on the front or back of the packages. Listed below are details regarding the recalled items: Product Description Size UPC Lot # Best By Date Sunrich Naturals Sunflower Kernel 1 oz. 37216074 14MAR17 37216075 15MAR17 37216076 16MAR17 37216077 17MAR17 37216078 18MAR17 37216081 21MAR17 37216082 22MAR17 37216083 23MAR17 37216084 24MAR17 37216085 25MAR17 37216088 28MAR17 37216090 30MAR17 37216091 31MAR17 37216092 01APR17 37216095 04APR17 37216096 05APR17 37216098 07APR17 37216099 08APR17 Planters Sunflower Kernels 3 oz. 029000012714 7072A3, 7072B3, 7072C3 03/13/17 7073A3, 7073B3, 7073C3 03/14/17 7074A3, 7074B3, 7074C3 03/15/17 7075A3 03/16/17 Recalled products were distributed to distribution centers during the months of March and April 2016 in California, Colorado, Connecticut, Florida, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Michigan, Minnesota, New Hampshire, New York, North Dakota, Ohio, Oregon, Pennsylvania and Texas and may be redistributed to other states nationwide. Consumers are urged not to consume these products. Consumers who purchased these products may take them back to the store where they purchased them for a refund or simply discard them. Consumers seeking information may email contactus@sunopta.com or call 1-888-886-4428 Monday through Friday, 8:00 a.m. to 5:00 p.m. Central Daylight Time. Retailers and wholesale customers should check their inventories and shelves to confirm that none of the recalled products are present or available for purchase by consumers or in warehouse inventories. Please contact SunOpta at contactus@sunopta.com to arrange for disposal or return of the product. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA). The Company provided the following statement: “SunOpta is committed to ensuring consumer safety and providing quality products and ingredients to customers. The Company has completed its root cause analysis and is working with food safety experts to implement corrective and preventative measures. In an abundance of caution, SunOpta is voluntarily extending the period during which it is recalling a limited number of sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes.” About SunOpta SunOpta Inc. is a leading global company focused on organic, non-genetically modified ("non-GMO") and specialty foods. SunOpta specializes in the sourcing, processing and packaging of organic and non-GMO food products, integrated from seed through packaged products; with a focus on strategic vertically integrated business models. SunOpta's organic and non-GMO food operations revolve around value-added grain, seed, fruit and vegetable based product offerings, supported by a global sourcing and supply infrastructure. Original Release http://www.fda.gov/Safety/Recalls/ucm499204.htm John
  22. http://www.fda.gov/Safety/Recalls/ucm501248.htm Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. The Quaker Oats Company Issues Voluntary Recall of Quaker Quinoa Granola Bars Due to Possible Health Risk For Immediate Release May 16, 2016 Contact Consumers 800-856-5781 Media Laura Ude Laura.Ude@pepsico.com (312) 821-2039 Announcement The Quaker Oats Company, a subsidiary of PepsiCo, Inc., today announced a voluntary recall of a small quantity of Quaker Quinoa Granola Bars after an ingredient supplier was found to have distributed sunflower kernels that may be contaminated with Listeria monocytogenes (L.mono). There have been no reported illnesses to date. However, Quaker is initiating the voluntary recall in an abundance of caution to protect public health. Listeria monocytogenes (L.mono) is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. While the vast majority of potentially affected Quaker products were withheld from ever reaching retail shelves, the products being recalled were distributed nationwide and are as follows: 6.1 ounce boxes of Quaker Quinoa Granola Bars Chocolate Nut Medley with UPC code 30000 32241 and Best Before Dates of: 10/16/2016, 10/17/2016 6.1 ounce boxes of Quaker Quinoa Granola Bars Yogurt, Fruit & Nut with UPC 30000 32243 and Best Before Dates of: 10/10/2016, 10/11/2016 Pictures of the products listed above will be available on www.quakeroats.com. At this time there are no other Quaker products involved in this situation. The company is working closely with the Food and Drug Administration (FDA) to further investigate this issue, but in the meantime is taking these actions out of commitment to and concern for consumers. Consumers who have purchased either of the above products are urged to dispose of or return them to the place of purchase for a full refund. They can also direct any questions to 800-856-5781, Monday – Friday, 8:30 a.m. – 6:00 p.m. (EST), or find more information at www.quakeroats.com. John
  23. http://www.fda.gov/Safety/Recalls/ucm500098.htm Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. NORPAC Foods, Inc. Recalls Natural Directions Organic Mixed Vegetables, And Natural Directions Organic Green Peas, Due To Possible Health Risk For Immediate Release May 9, 2016 Contact Consumers Consumer Affairs 888-641-9349 Media Amy Wood 971-275-3975 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm500098.htm#recall-photos NORPAC Foods, Inc. of Salem, Oregon is voluntarily recalling two (2) frozen private label vegetable items, Natural Directions Organic Mixed Vegetables and Natural Directions Organic Green Peas, because they have the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriage and stillbirths among pregnant women. This voluntary action is being undertaken because the recalled products contain vegetables that were purchased from CRF Frozen Foods and are part of the recent CRF Frozen Foods recall. No illnesses have been reported to date in connection with affected products listed in the table below. No other NORPAC retail branded products are affected by this recall. UPC Product Net Weight USE BY / SELL BY DATE Code UPC # 0-15400-19672-7 Natural Directions Organic Mixed Vegetables 12oz USE BY 06 2017 / MFG 06 16 2015 5J5 16X8 HH:MM USE BY 02 2018 / MFG 02 16 2016 5F6 16X8 HH:MM USE BY 04 2018 / MFG 04 19 2016 5H6 19X8 HH:MM UPC # 0-15400-19670-3 Natural Directions Organic Green Peas 12oz USE BY 03 2018 / MFG 03 21 2016 5G6 21X8 HH:MM USE BY 04 2018 / MFG 04 11 2016 5H6 11X8 HH:MM USE BY 04 2018 / MFG 04 12 2016 5H6 12X8 HH:MM All retailers who received the products have been contacted. Products being recalled may have been purchased in the states of: AK, CA, HI, ID, MT, NV, OR, WA, and Guam. Consumers who purchased these products may return them to the store where they were purchased for a refund, or simply discard them. Consumers with questions may call the company contact at 888-641-9349, Monday through Friday, 8:00 am to 5:00 pm PDT. FDA Investigates Listeria Outbreak Linked to Frozen Vegetables http://www.fda.gov/Food/RecallsOutbreaksEmergencies/Outbreaks/ucm499157.htm John
  24. http://www.fda.gov/Safety/Recalls/ucm499795.htm Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Harris Teeter Voluntarily Recalls Harris Teeter Frozen Organic Corn and Harris Teeter Frozen Mixed Vegetables For Immediate Release May 6, 2016 Contact Consumers CRF Recall Call Center 844-551-5595 Media Danna Robinson drobinson@harristeeter.com 704-844-3904 Lea Ramsey lmramsey@harristeeter.com 704-844-3209 Announcement Out of an abundance of caution, Harris Teeter is voluntarily recalling Harris Teeter Frozen Organic Corn and Harris Teeter Frozen Mixed Vegetables due to the potential for these products to be contaminated with Listeria monocytogenes. Harris Teeter was notified by Seabrook Brothers, the manufacturer of these products, may have used vegetables that are part of the recent CRF Frozen Foods recall. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. The recall applies to: Harris Teeter Frozen Organic Corn UPC number 7203676395 Harris Teeter Frozen Organic Mixed Vegetables UPC number 7203676393. Harris Teeter stocks Harris Teeter Frozen Organic Corn and Harris Teeter Frozen Mixed Vegetables. However, they do not currently stock the UPC’s listed above. These products may have been sold in Harris Teeter stores between October 19, 2015 and December 24, 2015. Harris Teeter asks customers who purchased the products containing the UPC’s mentioned between October 19, 2015 and December 24, 2015 to please not consume the products. Instead, please return the products to Harris Teeter for a full refund. Product quality and integrity are paramount to Harris Teeter.  If you purchased the recalled product, please return it to any Harris Teeter store for a full refund. Customers with questions should call CRF Frozen Foods at the CRF Recall Call Center at 844-551-5595. harristeeter.com Harris Teeter, with headquarters in Matthews, N.C., is a wholly-owned subsidiary of The Kroger Co. (NYSE: KR). The regional grocery chain employs approximately 28,000 associates and operates stores in North Carolina, South Carolina, Virginia, Georgia, Maryland, Delaware, Florida and the District of Columbia. Core Release http://www.fda.gov/Food/RecallsOutbreaksEmergencies/Outbreaks/ucm499157.htm John
  25. http://www.fda.gov/Safety/Recalls/ucm499122.htm Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Blue Bell Ice Cream Recalls Mispackaged Rocky Road Pints That Contain Cookies 'N Cream Ice Cream; Potential Allergy Concerns For Those With Wheat and Soy Allergies For Immediate Release May 3, 2016 Contact Consumers Blue Bell Ice Cream 979-836-7977 Media Jenny Van Dorf media@bluebell.com 979-830-9830 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm499122.htm#recall-photos Blue Bell Ice Cream is voluntarily recalling select lots of Rocky Road pints produced in its Brenham, Texas, plant because they may be mispackaged and actually contain Cookies 'n Cream Ice Cream. That ice cream contains the undeclared allergens soy and wheat, which may present a serious or life-threatening allergic reaction risk to people who have an allergy or severe sensitivity to soy or wheat. No illnesses have been reported to date, and there are no other health or safety concerns except for those posed to people that have soy or wheat allergies. A Blue Bell employee discovered the incorrect packaging while restocking a retailer. The pints can be identified as a Rocky Road pint with a Cookies 'n Cream lid, and contain Cookies 'n Cream Ice Cream. They can also be identified by the following code located on the bottom of the pint: 022918576. A picture of the affected product is included below. The ice cream pints were distributed in Texas and Louisiana through retail outlets, including food service accounts, convenience stores and supermarkets. PRODUCT: Rocky Road Ice Cream pints with Cookies 'n Cream lid and Cookies 'n Cream product. CODE DATE: 022918576 Consumers who have purchased these items can return them to the place of purchase for a full refund. For more information, consumers with questions may call 979-836-7977, Monday – Friday 8 a.m. – 5 p.m. CST. John
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