1,523 recalls · Class III, newest first
Reason Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of…
Reason Impurities/Degradation Products: This lot of product will not meet the impurity specification over shelf life
Reason Contraceptive Tablets Out of Sequence: This recall has been initiated due to the potential that some regimen packages may not contain placebo tablets.
Reason Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Reason Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Reason Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Reason Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Reason Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.
Reason Short Fill: The product is being recalled due to a potential underfill of the affected vials.
Reason Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.
Reason Failed USP Dissolution Test Requirements: Possible out-of-specification dissolution results at the 8 hour stability testing point.
Reason Failed USP Dissolution Test Requirements: Possible out-of-specification dissolution results at the 8 hour stability testing point.
Reason Subpotent (Single Ingredient Drug): The firm is recalling the product because the product is subpotent and does not meet the labeled 0.25% zinc…
Reason Subpotent (Single Ingredient Drug): out-of-specification result for coal tar content assay.
Reason Labeling Illegible: Missing Label; The voluntary recall of the aforementioned batch of product is being initiated due to two bottles missing…
Reason CGMP Deviations: tubing used for filling may interact with the nasal formulation of this product.
Reason Presence of Foreign Tablets/Capsules: One bottle of Percocet 10/325 mg was found to contain a tablet of Endocet 10/25 mg, the generic form.
Reason Subpotent (Single ingredient) drug : This is a sub recall of Teva's Enjuvia due to low Out of Specification (OOS) assay results.
Reason Subpotent (Single ingredient) drug : This is a sub recall of Teva's Enjuvia due to low Out of Specification (OOS) assay results.
Reason Subpotent (Single ingredient) drug : This is a sub recall of Teva's Enjuvia due to low Out of Specification (OOS) assay results.
Reason Chemical Contamination: QS Plus wipes were found to be contaminated with different substance (7820, Graffiti Remover).
Reason Chemical Contamination: Uncharacteristic moldy odor due to presence of 2,4,6-tribromoanisole (TBA).
Reason Labeling: Correct Labeled Product Miscart/Mispack: The shipper label displayed "5 mL x 50," instead of "10 mL x 50,"