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

676 recalls · Class II, newest first

Class II · Moderate risk

Ultra Violette

Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.

Ongoing Wrong potency / content Grace & Fire Pty LTD NDC 84803-106-01 D-0640-2025
Class II · Moderate risk

Sulfamethoxazole and Trimethoprim Tablets

Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No micro-organism was detected on any tablets.

Ongoing Particulate / foreign matter Northwind Pharmaceuticals LLC NDC 51655-307-87 D-0654-2025
Class II · Moderate risk

Carvedilol Tablets USP

CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm

Ongoing Nitrosamine impurity The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories NDC 0904-7307-61 D-0594-2025
Class II · Moderate risk

Dextroamphetamine Saccharate

Presence of Foreign Tablet/Capsule: Two (2) bottles labeled as Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 10mg, 100ct, contained one (1) tablet of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 5 mg.

Completed Particulate / foreign matter Lannett Company Inc. NDC 0527-0762-37 D-0642-2025
Class II · Moderate risk

chlorproMAZINE Hydrochloride Tablets

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

Ongoing Particulate / foreign matter Amneal Pharmaceuticals, LLC NDC 69238-1062-1 D-0619-2025
Class II · Moderate risk

chlorproMAZINE Hydrochloride Tablets

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

Ongoing Particulate / foreign matter Amneal Pharmaceuticals, LLC NDC 69238-1060-1 D-0618-2025
Class II · Moderate risk

chlorproMAZINE Hydrochloride Tablets

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

Ongoing Particulate / foreign matter Amneal Pharmaceuticals, LLC NDC 69238-1058-1 D-0617-2025
Class II · Moderate risk

chlorproMAZINE Hydrochloride Tablets

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

Ongoing Particulate / foreign matter Amneal Pharmaceuticals, LLC NDC 69238-1056-1 D-0616-2025
Class II · Moderate risk

Sulfamethoxazole and Trimethoprim Tablets

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

Ongoing Particulate / foreign matter Amneal Pharmaceuticals, LLC NDC 65162-272-10 D-0615-2025
Class II · Moderate risk

Lisdexamfetamine Dimesylate Capsules

Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate Capsules 40mg, contained Lisdexamphetamine Dimesylate Capsules 30mg.

Terminated Labeling / mix-up Lannett Company Inc. NDC 0527-4664-37 D-0599-2025
Class II · Moderate risk

Theophylline extended-release tablets 400mg

Failed Dissolution Specifications: Failure results (above) were reported for the Dissolution (by UV) test for commercial annual stability at the long-term shelf life stability interval, wherein the dissolution results do not comply with L3 stage dissolution criteria.

Ongoing Dissolution failure Glenmark Pharmaceuticals Inc., USA NDC 68462-380-01 D-0583-2025
Class II · Moderate risk

Carvedilol Tablets

CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.

Ongoing Nitrosamine impurity Glenmark Pharmaceuticals Inc., USA NDC 68462-165-05 D-0579-2025
Class II · Moderate risk

Carvedilol Tablets

CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.

Ongoing Nitrosamine impurity Glenmark Pharmaceuticals Inc., USA NDC 68462-164-05 D-0578-2025
Class II · Moderate risk

Carvedilol Tablets

CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.

Ongoing Nitrosamine impurity Glenmark Pharmaceuticals Inc., USA NDC 68462-162-05 D-0577-2025
Class II · Moderate risk

Carvedilol Tablets

CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm

Ongoing Nitrosamine impurity Glenmark Pharmaceuticals Inc., USA D-0588-2025
Class II · Moderate risk

Carvedilol Tablets

CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm

Ongoing Nitrosamine impurity Glenmark Pharmaceuticals Inc., USA NDC 68462-164-05 D-0587-2025
Class II · Moderate risk

Metoprolol Tartrate Tablets

CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.

Ongoing Nitrosamine impurity Westminster Pharmaceuticals LLC NDC 69367-355-10 D-0582-2025
Class II · Moderate risk

Metoprolol Tartrate Tablets

CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.

Ongoing Nitrosamine impurity Westminster Pharmaceuticals LLC NDC 69367-354-10 D-0581-2025

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