Recall Information from FDA https://www.fda.gov/AboutFDA/ContactFDA/StayInformed/RSSFeeds/Recalls/rss.xml en-us Wed, 24 Apr 2019 20:13:00 -0400 tina.gilliam@fda.hhs.gov Legacy Pharmaceutical Packaging, LLC is expanding its consumer-level recall of 3 repackaged lots Losartan Tablets USP 50mg to include one additional lot. Wed, 24 Apr 2019 20:13:00 -0400 https://www.fda.gov/Safety/Recalls/ucm636624.htm https://www.fda.gov/Safety/Recalls/ucm636624.htm This recall has been initiated due to an out of specification result for clarity observed in the stability program. The presence of the aluminum phosphate precipitate presents a potential risk that intravascular (I.V.) injection of product containing this precipitate could result in blood vessel in Wed, 24 Apr 2019 17:24:00 -0400 https://www.fda.gov/Safety/Recalls/ucm636617.htm https://www.fda.gov/Safety/Recalls/ucm636617.htm Alvogen, Inc. is voluntarily recalling two lots of Fentanyl Transdermal System 12 mcg/h transdermal patches to the consumer level. Sun, 21 Apr 2019 14:26:00 -0400 https://www.fda.gov/Safety/Recalls/ucm636384.htm https://www.fda.gov/Safety/Recalls/ucm636384.htm Torrent Pharmaceuticals Limited is expanding its recall for Losartan Potassium Tablets USP and Losartan Potassium/hydrochlorothiazide tablets, USP, to the consumer level due to the detection of trace amounts of an unexpected impurity found in an active pharmaceutical ingredient (API) manufactured by Hetero Labs Limited. The Recall is expanded to include an additional 36 lots of Losartan potassium Tablets USP and 68 lots of Losartan Potassium/Hydrochlorothiazide Tablets, USP Thu, 18 Apr 2019 17:55:00 -0400 https://www.fda.gov/Safety/Recalls/ucm636296.htm https://www.fda.gov/Safety/Recalls/ucm636296.htm Weis Markets today said it has issued a recall for its Weis Quality Banana Puddin Ice Cream (48oz) since the product’s ingredient label fails to list an egg allergen due to a supplier error. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume these products. There have been no reports of illness from customer’s consuming this product to date. Wed, 17 Apr 2019 19:06:00 -0400 https://www.fda.gov/Safety/Recalls/ucm636231.htm https://www.fda.gov/Safety/Recalls/ucm636231.htm Mondelēz Global LLC announced today a limited voluntary recall in the United States of certain Chewy Chips Ahoy 13oz cookies. This voluntary recall is being conducted because of the potential for certain product to contain an unexpected solidified ingredient. Some reports of potential adverse health effects have been received. Wed, 17 Apr 2019 14:37:00 -0400 https://www.fda.gov/Safety/Recalls/ucm636197.htm https://www.fda.gov/Safety/Recalls/ucm636197.htm Jensen Tuna of Louisiana is Voluntarily Recalling Frozen Ground Tuna Imported from JK Fish, Because it may Potentially be Contaminated with Salmonella. The frozen product, individually packaged in clear plastic one-pound bags, is sold in white wax 20 lb. boxes. The product is only sold as a wholesale case with twenty bags in each case. The lot numbers are z266, z271 and z272. Tue, 16 Apr 2019 16:45:00 -0400 https://www.fda.gov/Safety/Recalls/ucm636166.htm https://www.fda.gov/Safety/Recalls/ucm636166.htm Hercules Candy LLC . of East Syracuse, NY, is recalling its 4 ounce packages of Cashew Brittle Bits because they may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product. The recalled Cashew Brittle Bits were distributed from the brick and mortar retail in East Syracuse and nationally through the website www.herculescandy.com. Tue, 16 Apr 2019 12:40:00 -0400 https://www.fda.gov/Safety/Recalls/ucm636107.htm https://www.fda.gov/Safety/Recalls/ucm636107.htm Unilever is voluntarily recalling a limited quantity of Ben & Jerry’s Coconut Seven Layer Bar bulk and Ben & Jerry’s Chunky Monkey pints, which may inadvertently contain tree nuts including almonds, Brazil nuts, and hazelnuts that are not declared in the ingredient list or allergy information list. Both affected products include a “Contains Walnuts” and a “May contain other tree nuts” label on the back of the pack. Persons who have an allergy or severe sensitivity to these undeclared tree nuts run the risk of a serious or life-threatening allergic reaction if they consume the recalled products. Tue, 16 Apr 2019 12:39:00 -0400 https://www.fda.gov/Safety/Recalls/ucm636119.htm https://www.fda.gov/Safety/Recalls/ucm636119.htm Caito Foods is voluntarily recalling fresh cut watermelon, fresh cut honeydew melon, fresh cut cantaloupe and fresh cut mixed fruit containing one of these melons, produced at the Caito Foods facility in Indianapolis because these products have the potential to be contaminated with Salmonella Carrau, 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. Fri, 12 Apr 2019 20:15:00 -0400 https://www.fda.gov/Safety/Recalls/ucm635948.htm https://www.fda.gov/Safety/Recalls/ucm635948.htm SD Import, LLC is voluntarily recalling all lots of Aphrodisiac, Capsules to the consumer level. The products have been found to be tainted with sildenafil. FDA analysis has found the product to be tainted with sildenafil. Sildenafil is an active pharmaceutical ingredient in FDA approved product used in the treatment of erectile dysfunction. The presence of sildenafil in Aphrodisiac capsules renders it an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall. Thu, 11 Apr 2019 18:15:00 -0400 https://www.fda.gov/Safety/Recalls/ucm635860.htm https://www.fda.gov/Safety/Recalls/ucm635860.htm Great American Marketing Company of Houston, Texas is recalling Ready to Eat Sandwiches, Wraps and Salads 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 and 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 still births among pregnant women. Wed, 10 Apr 2019 17:55:00 -0400 https://www.fda.gov/Safety/Recalls/ucm635767.htm https://www.fda.gov/Safety/Recalls/ucm635767.htm Brian Richardson DBA “In Tha Pink”, is voluntarily recalling lots with the expiration of October 13, 2020 (13/10/2020) of ground Kopi Jantan Tradisional Natural Herbs Coffee to the consumer level. FDA analysis has found the product to be tainted with Sildenafil and Tadalafil Mon, 08 Apr 2019 15:18:00 -0400 https://www.fda.gov/Safety/Recalls/ucm635520.htm https://www.fda.gov/Safety/Recalls/ucm635520.htm Thogersen Family Farm of Stanwood, WA is voluntarily recalling raw frozen ground pet food because it has the potential to be contaminated with Listeria monocytogenes. The following varieties, packaged in two pound packs, are included in this recall: course ground rabbit, course ground mallard duck, ground llama, and ground pork frozen raw pet food Sat, 06 Apr 2019 20:07:00 -0400 https://www.fda.gov/Safety/Recalls/ucm635396.htm https://www.fda.gov/Safety/Recalls/ucm635396.htm Conagra Brands, Inc. (NYSE: CAG) is voluntarily recalling a limited amount of Hunt’s Tomato Paste No Salt Added six ounce cans. After the canning process, the final product could have been damaged, creating the potential for mold. Conagra Brands became aware of the issue after receiving calls from consumers. Thu, 04 Apr 2019 17:45:00 -0400 https://www.fda.gov/Safety/Recalls/ucm635309.htm https://www.fda.gov/Safety/Recalls/ucm635309.htm Wakefern Food Corp. has initiated a voluntary recall of a variety of Wholesome Pantry Organic nut butters because they may 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. No illnesses related to the recall have been reported. Tue, 02 Apr 2019 14:14:00 -0400 https://www.fda.gov/Safety/Recalls/ucm635086.htm https://www.fda.gov/Safety/Recalls/ucm635086.htm Little Red Rooster Ice Cream Company, d/b/a NadaMoo! (“NadaMoo!”) announced a limited voluntary recall of approximately 26,000 pints of its Strawberry Cheesecake Non-Dairy Frozen Dessert because they contain an undeclared almond ingredient. People who have an allergy or severe sensitivity to almonds run the risk of a serious or life-threatening allergic reaction if they consume the recalled products. Mon, 01 Apr 2019 18:55:00 -0400 https://www.fda.gov/Safety/Recalls/ucm634969.htm https://www.fda.gov/Safety/Recalls/ucm634969.htm Out of an abundance of caution, Nestle Purina PetCare Company is voluntarily recalling a limited amount of Muse wet cat food Natural Chicken Recipe in Gravy in three-ounce cans. The product could contain rubber pieces that are translucent yellow with a blue backing, which may present a potential choking hazard. Fri, 29 Mar 2019 20:00:00 -0400 https://www.fda.gov/Safety/Recalls/ucm634850.htm https://www.fda.gov/Safety/Recalls/ucm634850.htm Thomas Hammer Coffee Roasters Inc. of Spokane, WA is recalling 15 loaves of Blueberry Bread 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 this product. Fri, 29 Mar 2019 08:29:00 -0400 https://www.fda.gov/Safety/Recalls/ucm634747.htm https://www.fda.gov/Safety/Recalls/ucm634747.htm Theo Chocolate of Seattle, WA is voluntarily recalling 3oz Sea Salt 70% Dark Chocolate bars (UPC 8 74492 00325 8) because they may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume this product. Thu, 28 Mar 2019 18:15:00 -0400 https://www.fda.gov/Safety/Recalls/ucm634713.htm https://www.fda.gov/Safety/Recalls/ucm634713.htm