Independent register of U.S. FDA drug recalls · updated Oct 13, 2026
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FDA Drug Recalls

14,806 recalls, newest first

Class III · Low risk

Donnatal

Labeling: Not elsewhere classified - Product label incorrectly lists Scopolamine Hydrocodone as an active ingredient on the side panel instead of Scopolamine Hydrobromide.

Terminated Labeling / mix-up Rx PAK NDC 59212-425-10 D-0053-2016

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