Dextroamphetamine Sulfate Extended Release Capsules
Failed Dissolution Specifications: The affected lots may not meet the specifications for dissolution over the product shelf life.
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Failed Dissolution Specifications: The affected lots may not meet the specifications for dissolution over the product shelf life.
Failed Dissolution Specifications: The affected lots may not meet the specifications for dissolution over the product shelf life.
Labeling: Error on Declared Strength. Product labeled to contain 150 mcg tablets actually contained 75 mcg tablets.
Superpotent (Single Ingredient Drug): salicylic acid
Labeling: Not elsewhere classified: On 12/12/11, DEA published a final rule in the Federal Register making this product a schedule IV (C-IV)controlled substance. This product is being recalled because this controlled product was not relabeled with the required "C-IV" imprint on the label for products distributed after the 06/11/12 deadline.
Discoloration: Ethambutol Tablets USP 400 mg have tablets cores that may be discolored.
Presence of Foreign Substance: Reports of gray smudges identified as minute stainless steel particulates were found in the recalled tablets.
Microbial Contamination of Non-Sterile Products: Arthritis Relief Cream failed microbiological specifications.
Lack of Assurance of Sterility; potential that a low level of endotoxins may be present in the diluent vials.
Subpotent; 22 month stability timepoint
Subpotent; 12 month stability timepoint
Presence of Particulate Matter; fibers identified as cellulose and polyvinyl
Presence of Particulate Matter; fibers identified as cellulose and polyvinyl
Lack of Assurance of Sterility: Complains of a loose crimp applied to the fliptop vial; and a missing stopper and flip cap were received and therefore sterility cannot be assured.
Product Lacks Stability: Out-of-specification (OOS) results were observed for assay and description in retain samples.
Failed Dissolution Test Requirements
Defective Container: Pump head detaching from the canister unit upon removal of the overcap.
Subpotent; 15 month stability (by mfr)
Presence of Particulate Matter: Visible particulate and particulate embedded in vials were observed during retain inspection.
Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10 mg, 20 mg and 40 mg may contain small glass particulates.
Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10 mg, 20 mg and 40 mg may contain small glass particulates.
Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10 mg, 20 mg and 40 mg may contain small glass particulates.
Labeling Illegible: Portions of the product labeling in the area of the dosing directions, the warnings & other information sections is obscured.
Lack of Assurance of Sterility: Product did not meet the criteria for container closure integrity testing during routine 24 month stability testing.
Adulterated Presence of Foreign Tablets: A customer complaint was received that a bottle of Tramadol HCl Tablets USP 50 mg contained some tablets of Metoprolol Tartrate Tablets USP, 50 mg.