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

25 recalls, newest first

Class I · High risk

SLIMFIT X capsules

Marketed without an approved NDA/ANDA: Product contains undeclared sibutramine and desmethylsibutramine.

Terminated Chemical / undeclared Jersey Shore Supplements, LLC D-0473-2017
Class I · High risk

MegaJex Herbal Supplement

Marketed without an Approved NDA/ANDA; product contains sildenafil and tadalafil which are active pharmaceutical ingredients in FDA approved drugs used to treat erectile dysfunction (ED)

Terminated Chemical / undeclared MS Bionic D-0472-2017
Class I · High risk

Ultimate Body Tox PRO capsules

Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine. The presence of sibutramine, a previously approved controlled substance that was removed from the U.S. market in October 2010 for safety reasons, in this tainted product renders it an unapproved drug for which safety and efficacy have not been established and therefore subject to recall.

Terminated Chemical / undeclared Ultimate Body Tox D-0210-2017
Class I · High risk

Skinny Bee Diet capsules

Marketed without an approved NDA/ANDA: presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and phenolphthalein.

Terminated Chemical / undeclared Love My Tru Body D-0223-2017
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

3rd DEGREE capsules

Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.

Terminated Chemical / undeclared Making It a Lifestyle D-0222-2017
Class II · Moderate risk

Cisatracurium Besylate Injection

Incorrect/ Undeclared Excipient: Firm is recalling product due to an incorrect statement of Preservative free on the individual carton label. The vial label and outer carton label contain the correct statement of 0.9% benzyl alcohol added as a preservative.

Terminated Chemical / undeclared Fresenius Kabi USA, LLC NDC 63323-417-10 D-0819-2016
Class II · Moderate risk

Mannitol I.V.

Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.

Terminated Chemical / undeclared Hospira Inc. D-0831-2016
Class II · Moderate risk

Aminosyn-PF

Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.

Terminated Chemical / undeclared Hospira Inc. D-0830-2016
Class II · Moderate risk

Dextrose Injection

Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.

Terminated Chemical / undeclared Hospira Inc. NDC 0409-7935-19 D-0829-2016
Class II · Moderate risk

Dextrose Injection

Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.

Terminated Chemical / undeclared Hospira Inc. NDC 0409-7936-19 D-0828-2016
Class II · Moderate risk

Dextrose Injection

Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.

Terminated Chemical / undeclared Hospira Inc. NDC 0409-7918-19 D-0827-2016

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