Dextroamphetamine Saccharate
Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.
Class III means the product is unlikely to cause harm but violates FDA labeling or manufacturing rules. These are the recalls you rarely hear about; pharmacies usually just swap the affected lot.
1,716 recalls, newest first.
Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.
Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.
Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.
Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.
Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.
DEFECTIVE CONTAINER: Desflurane Liquid for Inhalation 240 mL may be leaking.
Out-of-specification organic impurity results obtained during routine stability testing.
Failed Impurities/Degradation - Out-of-specification results for Fluocinolone Acetonide impurity.
Failed Impurties/Degradation Specifications: out of specification results for an impurity for one lot
Presence of Foreign Tablets/Capsules: Metformin 1000mg with different imprint was found in bottles.
Subpotent Drug: Product testing identified a decreased level of the active ingredient, Cysteamine HCl.
Labeling: Product Contains Undeclared API; Incorrect formulation
Subpotent Drug
Failed Impurities/Degradation Specifications; high out of specification results obtained at the 9 month stability timepoint
Labeling: Incorrect or Missing Package Insert: The package insert included in the finished product is for the Canadian market and is not part of the current approved drug labeling.
Failed Stability Specifications: Out-of-Specification (OOS) results for the Aspirin related compound Salicylic Acid was observed.
Failed Stability Specifications: Out-of-Specification (OOS) results for the Aspirin related compound Salicylic Acid was observed.
Labeling; Not Elsewhere Classified: The Mentholatum Company is initiating a voluntary recall due to an error in the labeling of the cotton pellet box found within the Red Cross Oral Pain blister pack. The cotton pellet box states that the product contains "Natural Eugenol Oil" in which it does not.
Failed Content Uniformity: bulk lot used to make these two lots was found to have failed content uniformity.
Failed Tablet/Capsule Specifications: Tablets are imprinted with the incorrect identification code.
Failed Content Uniformity: bulk lot used to make these two lots was found to have failed content uniformity.
Labeling Error: Label Error on Declared Strength: Carton label and product insert incorrectly states the quantity of the excipient edetate disodium (EDTA) as 5.4 mg / vial, rather than the actual amount of 18.8 mg / vial.
Cross contamination with other products - OOS discovered during routine stability testing for highest unknown impurity later identified as clozapine
SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.
SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.