Independent register of U.S. FDA drug recalls · updated Oct 13, 2026
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FDA Drug Recalls

14,806 recalls, newest first

Class III · Low risk

Testosterone Topical Solution

Defective Container: Repetitive complaints received indicating pump not working.

Terminated Packaging defect Lupin Pharmaceuticals Inc. NDC 68180-943-11 D-1010-2019
Class II · Moderate risk

Red Eye

Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.

Terminated Sterility / contamination MSM Nutraceuticals, LLC D-1128-2019
Class II · Moderate risk

Dry Eye

Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.

Terminated Sterility / contamination MSM Nutraceuticals, LLC D-1127-2019
Class II · Moderate risk

15% Msm

Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.

Terminated Sterility / contamination MSM Nutraceuticals, LLC D-1126-2019
Class II · Moderate risk

Volumex (Iodinated I 131 Albumin)

Lack of Assurance of Sterility: preliminary environmental monitoring report exceeds limits, therefore sterility cannot be assured.

Terminated Sterility / contamination Iso-Tex Diagnostics, Inc NDC 50914-7720-8 D-1008-2019
Class III · Low risk

Mirapex (pramipexole dihydrochloride)

Failed Tablet/Capsule Specifications: identification of low weight tablets during routine stability testing.

Terminated Failed specification Boehringer Ingelheim Pharmaceuticals, Inc. NDC 0597-0190-61 D-0991-2019
Class II · Moderate risk

Losartan Potassium Tablets

CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified.

Terminated Nitrosamine impurity Preferred Pharmaceuticals, Inc D-1051-2019
Class II · Moderate risk

Valsartan Tablets USP 160 mg

CGMP Deviation: Presence of NDEA (N-Nitrosodimethylamine), a carcinogen impurity, detected in the active ingredient.

Terminated Nitrosamine impurity American Health Packaging D-1047-2019
Class II · Moderate risk

Docetaxel Injection USP

Defective Container: complaint for seal and cap vial issues that could lead to a lack of sterility assurance.

Terminated Packaging defect Dr. Reddy's Laboratories, Inc. NDC 43598-259-40 D-1001-2019
Class I · High risk

LEOPARD Miracle Honey packaged in a wooden box

Marketed Without An Approved NDA/ANDA: product tainted with undeclared sildenafil, an FDA approved drug for the treatment of male erectile dysfunction. The presence of sildenafil in Leopard Miracle Honey renders it an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.

Terminated Chemical / undeclared USA LESS Inc. D-1135-2019

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