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

1,563 recalls, newest first

Class I · High risk

Ketorolac Trom

Presence of Particulate Matter: Medication relabeled at facility was recalled by the manufacturer due to small black particles noticed during routine visual inspection. of retain samples.

Terminated Particulate / foreign matter RemedyRepack Inc. NDC 70518-1239-00 D-0867-2020
Class II · Moderate risk

Sumatriptan Succinate Tablets

Failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance.

Terminated Impurity / degradation Sun Pharmaceutical Industries, Inc. D-0660-2020
Class II · Moderate risk

Sumatriptan Succinate Tablets

Failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance.

Terminated Impurity / degradation Sun Pharmaceutical Industries, Inc. NDC 62756-521-69 D-0659-2020
Class II · Moderate risk

Blisovi Fe 1.5/30

Failed Tablet/Capsule Specifications: Complaints related to crumbling of tablets when popped out of the blister pack.

Terminated Failed specification Lupin Pharmaceuticals Inc. NDC 68180-866-11 D-0638-2020
Class II · Moderate risk

Theraflu Cough Relief

Labeling: Label Lacks Warning: Product recalled due to absence of a warning statement on the product label, Ask a doctor before use if you have a sodium-restricted diet.

Terminated Labeling / mix-up GSK Consumer Health, Inc D-0996-2020
Class I · High risk

Lamotrigine Tablets

Cross Contamination; Lamotrigine Tablets 100 mg USP was contaminated with enalapril maleate.

Terminated Cross-contamination Taro Pharmaceuticals U.S.A., Inc. NDC 51672-4131-1 D-0833-2020
Class II · Moderate risk

Ranitidine Tablets

CGMP Deviations: Presence of NDMA impurity detected in product.

Terminated Nitrosamine impurity Denton Pharma, Inc. NDC 70934-287-15 D-0795-2020
Class II · Moderate risk

Ranitidine Tablets

CGMP Deviations: Presence of NDMA impurity detected in product.

Terminated Nitrosamine impurity Denton Pharma, Inc. NDC 70934-017-04 D-0794-2020

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