cGMP Deviations: Product manufactured with contaminated raw ingredient.
Precision Dose
cGMP Deviations: Product manufactured with contaminated raw ingredient.
cGMP deviations: The firm was notified of the manufacturer's expanded recall.
CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API.
Subpotent Drug: low out of specification results.
Class I - Dangerous
Labeling Error: Label mix-up. Products' unit dose cups are correctly labeled, but the product carton lists incorrect volume and NDC.
Labeling: Not Elsewhere Classified: This unit dose product is being recalled because the product's name includes the word "Children's" which is misleading since the 650 mg dose of acetaminophen contained within it, is an adult dose.