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

526 recalls, newest first

Class I · High risk

ForeverMen Natural Energy Boost Capsules

Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this unapproved drug.

Terminated Chemical / undeclared FA Online Inc D-0470-2024
Class I · High risk

WEFUN Capsules 825 mg

Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil, an ingredient found in a FDA approved product for the treatment of male sexual enhancement, making this an unapproved drug.

Terminated Chemical / undeclared Hua Da Trading, Inc. dba Wefun Inc. D-1180-2023
Class II · Moderate risk

Isopropyl Alcohol Antiseptic 75%

CGMP deficiencies: Product manufactured at the same site where FDA testing found Presence of methanol in other products.

Terminated Chemical / undeclared Jarman's Midwest Cleaning Systems, Inc. D-0872-2023
Class I · High risk

PrimeZEN Black 6000 capsule

Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Terminated Chemical / undeclared Volt Candy Wholesale Club D-0453-2023
Class II · Moderate risk

Proton Armor

Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.

Terminated Chemical / undeclared Ultra Chem Labs Corp NDC 79208-001-50 D-0017-2023
Class II · Moderate risk

Proton Armor

Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.

Terminated Chemical / undeclared Ultra Chem Labs Corp NDC 79208-001-50 D-0016-2023
Class I · High risk

Launch Sequence Aphrodisia Capsules

Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Terminated Chemical / undeclared Loud Muscle Science D-1338-2022
Class I · High risk

Launch Sequence Euphoria Capsules

Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Terminated Chemical / undeclared Loud Muscle Science D-1337-2022
Class I · High risk

Launch Sequence Capsules

Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Terminated Chemical / undeclared Loud Muscle Science D-1336-2022
Class III · Low risk

Wal-Tussin DM

Incorrect/Undeclared Excipient: Product contains alcohol

Terminated Chemical / undeclared AptaPharma Inc. NDC 0363-0324-28 D-0787-2022
Class I · High risk

Pink Pussycat SENSUAL ENHANCEMENT capsule

Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Terminated Chemical / undeclared Pink Toyz D-0785-2022
Class II · Moderate risk

HAND SANITIZER Isopropyl Alcohol Antiseptic 75%

CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.

Terminated Chemical / undeclared Tennessee Technical Coatings, Corp. NDC 76921-000-01 D-0740-2022

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