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

1 recalls · Class III, newest first

Class III · Low risk

V-FORCE Homeopathic

Incorrect Product Formulation: product contains Active Ingredient Glandula Suprarenalis Suis 8X instead of Glandula Suprarenalis Bovine 8X (as stated on the product label).

Terminated cGMP deviation Grato Holdings, Inc. D-0099-2024

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