Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA Drug Recalls

14,806 recalls, newest first

Class II · Moderate risk

Eye Drops advanced relief

Labeling: Label Mix-Up: Incorrect back labeling of the immediate container of eye drops (unit carton and front label are correct) which do not list three active ingredients: Dextran 70, PEG 400, and povidone.

Terminated Labeling / mix-up K C Pharmaceuticals Inc D-192-2013
Class II · Moderate risk

Leflunomide tablets

Subpotent (Single Ingredient Drug): Distribution of product that did not meet specifications.

Terminated Wrong potency / content Apotex Corp. NDC 60505-2503-3 D-1662-2012
Class II · Moderate risk

Leflunomide tablets

Subpotent (Single Ingredient Drug): Distribution of product that did not meet specifications.

Terminated Wrong potency / content Apotex Corp. NDC 60505-2502-1 D-1661-2012

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