US Drug Recall Register

FDA Drug Recalls

17,898 recalls, newest first

Class I · High risk Ongoing

Cyclobenzaprine Hydrochloride Tablets

Reason Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets (yellow in color), were labeled as Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (blue in color).

Unichem Pharmaceuticals USA Inc. NDC 29300-415-19 D-0655-2025
Class II · Moderate risk Ongoing

chlorproMAZINE Hydrochloride Tablets

Reason Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was detected on any tablets.

Amerisource Health Services LLC D-0650-2025
Class II · Moderate risk Ongoing

chlorproMAZINE Hydrochloride Tablets

Reason Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was detected on any tablets.

Amerisource Health Services LLC D-0649-2025
Class II · Moderate risk Ongoing

chlorproMAZINE Hydrochloride Tablets

Reason Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was detected on any tablets.

Amerisource Health Services LLC D-0648-2025
Class II · Moderate risk Ongoing

chlorproMAZINE Hydrochloride Tablets

Reason Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was detected on any tablets.

Amerisource Health Services LLC D-0647-2025
Class II · Moderate risk Ongoing

Neuroquell & Neuroquell Plus

Reason cGMP violations

Atlantic Management Resources Ltd. D-0629-2025
Class II · Moderate risk Ongoing

Succinylcholine Chloride Injection

Reason Failed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation impurity.

Zydus Pharmaceuticals (USA) Inc NDC 70710-1377-1 D-0623-2025
Class II · Moderate risk Ongoing

UltraSure Anti-Perspirant & Deodorant

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-266-04 D-0177-2026
Class II · Moderate risk Ongoing

San-E-Foam

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-107-34 D-0176-2026
Class II · Moderate risk Ongoing

Renew Skin Repair Cream

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-405-05 D-0175-2026
Class II · Moderate risk Ongoing

Renew PeriProtect

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-435-04 D-0174-2026
Class II · Moderate risk Ongoing

PeriGuard Ointment

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-205-05 D-0173-2026
Class II · Moderate risk Ongoing

PeriGiene

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-198-08 D-0172-2026
Class II · Moderate risk Ongoing

McKesson Skin Protectant

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 68599-6202-1 D-0171-2026
Class II · Moderate risk Ongoing

Lantiseptic

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-304-05 D-0170-2026
Class II · Moderate risk Ongoing

Lantiseptic

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-504-05 D-0169-2026
Class II · Moderate risk Ongoing

KleenFoam Antimicrobial Foam Soap

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-093-34 D-0168-2026
Class II · Moderate risk Ongoing

Hand-E-Foam

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-102-08 D-0167-2026
Class II · Moderate risk Ongoing

GelRite Instant Hand Sanitizer

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-106-04 D-0166-2026
Class II · Moderate risk Ongoing

DermaSarra

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-189-08 D-0165-2026
Class II · Moderate risk Ongoing

DermaMed Ointment

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-214-04 D-0164-2026
Class II · Moderate risk Ongoing

DermaKleen

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-092-08 D-0163-2026
Class II · Moderate risk Ongoing

DermaFungal

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-234-05 D-0162-2026
Class II · Moderate risk Ongoing

DermaCerin

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-174-04 D-0161-2026
Class II · Moderate risk Ongoing

4-N-1 Skin Protectant

Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

DermaRite Industries, LLC NDC 61924-208-04 D-0160-2026