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

18,003 recalls, newest first

Class I · High risk

Super Samurai-X

Marketed without an approved NDA/ANDA: FDA sample analyses revealed the presence of undeclared sildenafil and/or its analogs in products marketed as dietary supplements

Terminated Chemical / undeclared SOS Telecom Inc. D-0104-2017
Class I · High risk

Ginseng Power-X

Marketed without an approved NDA/ANDA: FDA sample analyses revealed the presence of undeclared sildenafil and/or its analogs in products marketed as dietary supplements

Terminated Chemical / undeclared SOS Telecom Inc. D-0103-2017
Class I · High risk

Ninja-X

Marketed without an approved NDA/ANDA: FDA sample analyses revealed the presence of undeclared sildenafil and/or its analogs in products marketed as dietary supplements

Terminated Chemical / undeclared SOS Telecom Inc. D-0102-2017
Class I · High risk

Tiger-X

Marketed without an approved NDA/ANDA: FDA sample analyses revealed the presence of undeclared sildenafil and/or its analogs in products marketed as dietary supplements

Terminated Chemical / undeclared SOS Telecom Inc. D-0101-2017
Class II · Moderate risk

tabcin NOCHE

CGMP Deviations

Terminated cGMP deviation Profarma Distributors LLC D-1040-2016
Class II · Moderate risk

Bromocriptine Mesylate Capsules USP

Failed impurities/degradation specifications: Out of specification results noticed in related substance test during analysis of 24 months long term (25 degree Celsius /65% RH) stability samples of two batches.

Terminated Impurity / degradation Zydus Pharmaceuticals USA Inc NDC 68382-110-06 D-1491-2016

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