FDA Warning & Recall Information

On January 18, 2023, Corim Industries announced a voluntary recall of four peanut butter hot chocolate products because they may contain peanuts not declared on the labeling, according to the FDA. The recall primarily affects people with allergies or severe sensitivities to peanuts, who would […]

The FDA is calling to attention a voluntary recall of Fullei Fresh’s alfalfa sprouts after Shiga toxin-producing E. coli (STEC) was detected in the finished product. The action was initiated by the company on January 19, 2023, and impacts products under a single lot (lot […]

On January 10, 2023, Daiso California, LLC recalled a dozen products under the brand names Tohato and Kashiwado after it was found that their packaging does not declare all allergen ingredients. The inadequate disclosure of allergens has consequences for people with an allergy or severe […]

On January 13, 2023, Glendale, New York-based Utopia Foods Inc. announced an expanded recall of its Enoki Mushrooms after the product was determined to be potentially contaminated by the organism Listeria monocytogenes. Though healthy individuals may experience only short-lived symptoms like “high fever, severe headache, […]

On January 13, 2023, the FDA updated a July 10, 2022 Class I recall of Intera Oncology’s Intera 3000 Hepatic Artery Infusion Pump to clarify that a failure to recognize and adjust the product’s faster-than-normal flow rates may result in major adverse health outcomes. Implanted […]

The FDA is calling to attention a Texas-wide recall of 976 pounds of brownies packaged under the product H-E-B Meal Simple Chocolate Chunk Brownie 13oz by Ameripack Foods, LLC. Announced by the Hughes Springs, Texas company on January 11, 2023, the action was made due […]

On December 30, 2022, Avery’s Savory Popcorn LLC recalled its Gourmet Popcorn, All Flavors, due to the possibility of the product containing a number of undeclared allergens, reports the FDA. The Dallas-based company initiated the recall after the product was found to have been shipped […]

Three lots of Epinephrine (L-Adrenaline) USP, a bulk active pharmaceutical ingredient (API) used in the manufacture of prescription products, are being voluntarily recalled to the user level by Spectrum Laboratory Products, Inc., according to the FDA. The company announced the move on January 9, 2023, […]

According to the FDA, four lots of Quinapril Tablets by Lupin Pharmaceuticals Inc. were voluntarily recalled to the consumer level on December 21, 2022. The action was made after recent testing found a nitrosamine impurity, N-Nitroso-Quinapril, which registered in excess of the Acceptable Daily Intake […]

On December 29, 2022, Caesar’s Pasta, LLC recalled 5,610 pounds of its frozen manicotti after a routine sampling program revealed the finished product might contain the bacteria Listeria monocytogenes, according to the FDA.  While the organism may cause healthy people to suffer only short-lived symptoms like […]

On December 12, 2022, Smith’s Medical sent out an Urgent Medical Device Correction Letter to customers after identifying two potential problems with its CADD Infusion System Infusion Sets, according to the FDA. Designed for use with CADD pumps (“multi-therapy infusion pumps for ambulatory medication delivery,” […]

On December 29, 2022, Sunsprout Enterprises voluntarily recalled four lots of raw alfalfa sprouts due to potential salmonella contamination. The action comes on the heels of a preliminary investigation conducted by the State of Nebraska and the CDC in response to an outbreak of illness […]