Independent register of U.S. FDA drug recalls · updated Oct 11, 2026
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FDA Drug Recalls

18,003 recalls, newest first

Class II · Moderate risk

Travoprost Ophthalmic Solution

Subpotent Drug and Failed Impurities/Degradation Specifications: low out-of-specification results obtained for assay and high out-of-specification results for related substance impurities/degradation during routine stability testing.

Terminated Impurity / degradation Mylan Pharmaceuticals Inc NDC 0378-9651-32 D-0748-2022
Class III · Low risk

23.4% Sodium Chloride Injection

Labeling: Incorrect Barcode: Product barcode incorrectly identifies the product as rocuronium bromide injection 100 mg per 10 mL instead of sodium chloride injection 23.4%, 120 mEq per 30 mL.

Terminated Labeling / mix-up The Ritedose Corporation D-0745-2022
Class III · Low risk

Wal-Tussin DM

Incorrect/Undeclared Excipient: Product contains alcohol

Terminated Chemical / undeclared AptaPharma Inc. NDC 0363-0324-28 D-0787-2022
Class I · High risk

Pink Pussycat SENSUAL ENHANCEMENT capsule

Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Terminated Chemical / undeclared Pink Toyz D-0785-2022
Class II · Moderate risk

Preferred Pharmaceuticals

Out of specification results observed in dissolution during long term stability testing.

Terminated Dissolution failure Preferred Pharmaceuticals, Inc. NDC 68788-6390-09 D-0769-2022
Class II · Moderate risk

Milk of Magnesia USP

CGMP Deviations: Failure to properly investigate failed microbial testing.

Completed Microbial contamination Plastikon Healthcare LLC NDC 0904-6846-73 D-0870-2022

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