FDA Drug Recalls
1,709 recalls · Class III, newest first
Class III · Low risk Terminated
Reason Labeling Illegible: Missing Label; The voluntary recall of the aforementioned batch of product is being initiated due to two bottles missing…
Class III · Low risk Terminated
Reason CGMP Deviations: tubing used for filling may interact with the nasal formulation of this product.
Class III · Low risk Terminated
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.
Class III · Low risk Terminated
Reason Subpotent (Single ingredient) drug : This is a sub recall of Teva's Enjuvia due to low Out of Specification (OOS) assay results.
Class III · Low risk Terminated
Reason Subpotent (Single ingredient) drug : This is a sub recall of Teva's Enjuvia due to low Out of Specification (OOS) assay results.
Class III · Low risk Terminated
Reason Subpotent (Single ingredient) drug : This is a sub recall of Teva's Enjuvia due to low Out of Specification (OOS) assay results.
Class III · Low risk Terminated
Reason Chemical Contamination: QS Plus wipes were found to be contaminated with different substance (7820, Graffiti Remover).
Class III · Low risk Terminated
Reason Chemical Contamination: Uncharacteristic moldy odor due to presence of 2,4,6-tribromoanisole (TBA).
Class III · Low risk Terminated
Reason Labeling: Correct Labeled Product Miscart/Mispack: The shipper label displayed "5 mL x 50," instead of "10 mL x 50,"