Food and Drugs Administration–Recalls/Safety Alerts

• Monkey Spit, LLC Issues Allergy Alert on Undeclared Milk/Wheat/Soy in Monkey Spit BBQ Sauces January 18, 2025
  People who have allergies to milk/wheat/soy run the risk of serious or life-threatening allergic reaction if they consume these products. The three recalled “Monkey Spit BBQ Sauces" were distributed locally in retail stores on the central coast of California and through mail orders on our website:
  FDA
• Wismettac Asian Foods Issues Allergy Alert on Undeclared Milk in Curvee Puffs Corn Puff Snack Curry Flavor January 17, 2025
  Wismettac Asian Foods, Inc., Santa Fe Springs, CA is recalling 2.46 oz packages of Shirakiku brand Curvee Puffs Corn Puff Snack Curry Flavor. The product contains the undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reacti
  FDA
• Mutual Trading Co., Issues Allergy Alert Undeclared Milk in Prepared Monkfish Liver January 15, 2025
  New York Mutual Trading Co., Inc of Secaucus, NJ is recalling 7.05 oz of Prepared Monkfish Liver (Ankimobo) because the package label contains undeclared milk allergen. People who have an allergy or severe sensitivity to milk allergen run the risk of serious or life-threatening allergic reaction if
  FDA
• Quaker Issues Limited Recall on Undeclared Milk in Pearl Milling Company Original Pancake & Waffle Mix Distributed in 11 States January 14, 2025
  January 14, 2025 – The Quaker Oats Company today issued a recall of a limited number of two pound boxes of Pearl Milling Company Original Pancake & Waffle Mix that may contain undeclared milk, after being alerted by a retail partner. Those with an allergy or severe sensitivity to milk run the risk o
  FDA
• Max Mobility / Permobil Issues Nationwide Recall of SmartDrive Speed Control Dial Due to the Motor Being Unresponsive to the User January 14, 2025
  Max Mobility/Permobil has initiated a nationwide recall of the Speed Control Dial component used with the SmartDrive MX2+ Power Assist Device due to potential safety and performance concerns.
  FDA
• Lifestyle Evolution Voluntarily Recalls NuGo Dark Chocolate Chip and NuGo Dark Pretzel Due to Undeclared Milk January 10, 2025
  Lifestyle Evolution Inc., is recalling select lots of NuGo Dark Chocolate Chip and Dark Chocolate Pretzel nutrition bars because they may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume
  FDA
• The Mochi Ice Cream Company LLC Issues Allergy Alert on Undeclared Egg in Peach Mango Sorbet January 9, 2025
  The Mochi Ice Cream Company LLC, Vernon, California is recalling 1350 cases of Peach Mango Sorbet, because it may contain undeclared pasteurized cooked egg white. People who have an allergy or severe sensitivity to eggs, run the risk of serious or life-threatening allergic reaction if they consume t
  FDA
• Blue Ridge Beef Recalls Blue Ridge Beef Kitten Mix Due to Salmonella Contamination January 4, 2025
  STATESVILLE, NC - January 3, 2025- Blue Ridge Beef is recalling 1,350 lbs. of their 2 1b log Kitten Mix Lot N25-0716 UPC 8542980013436 due to a contamination of Salmonella. (Lot numbers are stamped in the clips on the end of the chubs/bags).
  FDA
• Dierbregs Markets Issues Allergy Alert on Undeclared Wheat in Product January 3, 2025
  Dierbergs is recalling all 16oz Premium Home-Style Mashed Potatoes with a Sell By Date of January 09, 2025. The product carries an undeclared allergen of Wheat. The affected product is identifiable by a label ID number of 92 in the lower left-hand corner above the UPC code.
  FDA
• Abbey Specialty Foods Recalls Wicklow Gold Cheddar Nettle & Chive 5.2 oz and Wicklow Gold Cheddar Tomato & Herb 5.2 oz Because of Possible Health Risk January 3, 2025
  Abbey Specialty Foods of Fairfield, NJ is recalling Wicklow Gold Cheddar Nettle & Chive 5.2 oz product and Wicklow Gold Cheddar Tomato & Herb 5.2 oz product because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infecti
  FDA
• Braga Fresh Issues Voluntary and Precautionary Advisory Due to Possible Health Risk December 27, 2024
  Soledad, Calif. – Dec. 27, 2024 – Braga Fresh is voluntarily issuing a precautionary advisory of a single production lot of washed and ready-to-eat 12oz Marketside Broccoli Florets with best if used by date.
  FDA
• Gardners Candies Issues Allergy Alert on Undeclared Tree Nuts in Cappuccino Meltaway® Bars and Gardners Meltaway Treat Boxes Containing Cappuccino Meltaway Bars December 27, 2024
  Gardners Candies of Tyrone, PA is recalling its 1.25 ounce packages of Gardners Candies brand Cappuccino Meltaway® Bars because they may contain undeclared tree nuts (cashews). People who have an allergy or severe sensitivity to tree nuts run the risk of serious or life-threatening allergic reaction
  FDA
• Astellas Pharma US, Inc. Issues Voluntary Nationwide Recall of One Lot of PROGRAF® 0.5mg (Tacrolimus) and One Lot of ASTAGRAF XL® 0.5mg (Tacrolimus Extended-Release Capsules) Because Bottles Shipped to U.S. May Contain Empty Capsules December 24, 2024
  Astellas Pharma US, Inc. (Head of US Commercial: Michael Petroutsas, "Astellas") is voluntarily recalling one lot of PROGRAF® 0.5mg (tacrolimus) and one lot of ASTAGRAF XL® 0.5mg (tacrolimus extended-release) capsules to the consumer level. These products are being recalled because bottles may conta
  FDA
• Alcon Laboratories Issues Voluntary Nationwide Recall of One (1) Lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101), Due to Fungal Contamination December 21, 2024
  Fort Worth, Texas. Alcon Laboratories is voluntarily recalling one (1) lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101) to the consumer level. Alcon evaluated a consumer complaint of foreign material observed inside a sealed single use vial and determined th
  FDA
• Lidl Recalls Taste of Deutschland Buttered Vegetables Due to Undeclared Milk Allergens December 20, 2024
  DECEMBER 20, 2024 – Lidl US is recalling all lots of their Taste of Deutschland Buttered Vegetables 10.5 oz box UPC 4 056489 122876 due to undeclared milk allergen. The recall was issued due to undeclared milk in the products. People who have allergies to milk run the risk of serious or life-threate
  FDA
• Endo USA, Inc. Issues Voluntary, Nationwide Recall of Adrenalin® Chloride Solution (EPINEPHrine Nasal Solution, USP) Due to the Potential for Administration Errors December 20, 2024
  Endo, Inc (OTCQX: NDOI) (“Endo”), announced today that one of its operating subsidiaries, Endo USA, Inc., is voluntarily recalling all lots within expiry of Adrenalin® Chloride Solution (EPINEPHrine nasal solution, USP) 30mg/30mL (1mg/mL) 30 mL vials, to the consumer level. This product, which pre-d
  FDA
• Recall of Jose Madrid Salsa Chipotle Con Queso December 20, 2024
  Jose Madrid Salsa is announcing a voluntary recall of our Chipotle Con Queso Salsa. The salsa is being recalled because it contains Yellow 5 and Yellow 6, which were not listed on the ingredient label. Individuals who are allergic or sensitive to Yellow 5 or Yellow 6 run the risk of minor to serious
  FDA
• Orgain Issues Voluntary Allergy Alert on Possible Undeclared Peanut Residue in a Single Batch of 30G Protein Organic Plant Based Powder – Chocolate 2.01lb December 19, 2024
  Orgain of Irvine, California is voluntarily recalling a single batch of its 30g Protein Organic Plant Based Powder - Chocolate 2.01lb because it may contain undeclared peanut residue. People who have an allergy or severe sensitivity to peanuts may run the risk of serious or life-threatening allergic
  FDA
• GNMART INC Issues Voluntary Nationwide Recall of Force Forever Due to Undeclared Drug Ingredients Diclofenac and Dexamethasone December 16, 2024
  12/12/2024, Dover Plains, NY, GNMART INC is voluntarily recalling all lots of Force Forever for joint Pain, 60 Tablets packaged in a white plastic bottle with a red cap, labeled as "FORCE FOREVER.", to the consumer level. FDA analysis has found product to contain undeclared Diclofenac and Dexamethas
  FDA
• Shoppers-Plaza Issues Voluntary Nationwide Recall of Fouzee Sugarlin Herbal Formula Due To Presence Of Undeclared Metformin And Glyburide December 16, 2024
  December 16, 2024 – Los Angeles, California - Shoppers-Plaza is voluntarily recalling all lots of Fouzee Sugarlin Herbal Formula capsules to the consumer level. See Attachment 1 for photo of product labeling. Fouzee Sugarlin Herbal Formula capsules is an unapproved new drug for which safety and effi
  FDA