All recalls8,521 total
Marketed without Approved NDA/ANDA. FDA analysis found product to be tainted with undeclared Diclofenac and Omeprazole.
Potential contamination with Listeria monocytogenes
Product may be contaminated with mold.
Product may be contaminated with mold.
Product may be contaminated with mold.
Undeclared gluten
Undeclared Fish Allergen
Failure of fusion system instruments in the field.
Failure of fusion system instruments in the field.
Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared Diclofenac and Omeprazole.
Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Undeclared Allergen - Wheat
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Undeclared peanuts
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Elevated levels of cadmium in plates
Potential to be contaminated with Salmonella
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information.
Product was recalled due to the temperature being over 40 degrees and not on ice July 1st, 2024
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled as 0.125 mg instead of 0.25 mg. The blister strips inside the product carton reflect the correct strength of 0.25 mg.
Customer complaint for bloated bottles. Testing and examination of these lots has revealed they did not meet specifications, including elevated pH and water activity levels. This may be indicative of microbiological activity, and concurrent risk of food-borne illness.
Customer complaint for bloated bottles. Testing and examination of these lots has revealed they did not meet specifications, including elevated pH and water activity levels. This may be indicative of microbiological activity, and concurrent risk of food-borne illness.
Undeclared Soy. Carrot Cake slices were inadvertently placed into some Chocolate Cake slice containers. The Chocolate Cake ingredient statement does not list the allergen soy which is in the Carrot Cake.