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

37 recalls, newest first

Class II · Moderate risk

Adam's Polishes ALCOHOL BASED HAND SANITIZER

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

Ongoing Chemical / undeclared Adam's Polishes LLC NDC 74943-125-04 D-0067-2023
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 I · High risk

Artri King Reforzado con Ortiga Omega 3 Tablets

Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.

Completed Chemical / undeclared Walmart Inc D-1157-2022
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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