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

18,003 recalls, newest first

Class III · Low risk

Amlodipine Besylate Tablets

Subpotent Drug: Out-of-Specification test results observed in assay test at 21-month long term stability study.

Terminated Wrong potency / content Lupin Pharmaceuticals Inc. NDC 68180-721-03 D-0899-2023
Class I · High risk

Tydemy

Failed Stability Specification and Failed Impurities/Degradation Specifications: out of specification for inactive content ascorbic acid and MTHFRC-7impurity test

Terminated Impurity / degradation Lupin Pharmaceuticals Inc. NDC 68180-904-71 D-1081-2023
Class II · Moderate risk

Tizanidine Tablets

Failed Dissolution Specifications: this repackaged product was recalled by the manufacturer, Dr. Reddy's Laboratories, Inc., due to out of specification results for dissolution.

Terminated Dissolution failure Amerisource Health Services LLC NDC 68084-645-01 D-0892-2023
Class II · Moderate risk

Tizanidine Tablets USP

Failed dissolution specification: Out of specification results observed in 24-month long term stability testing.

Ongoing Dissolution failure Dr Reddy's Laboratories Limited NDC 55111-180-10 D-0923-2023
Class II · Moderate risk

Dry Eye Relief Lubricant Eye Drops

CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.

Ongoing cGMP deviation K.C. Pharmaceuticals, Inc NDC 49035-280-02 D-0898-2023
Class II · Moderate risk

Original Eye Drops

CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.

Ongoing cGMP deviation K.C. Pharmaceuticals, Inc NDC 49348-037-29 D-0897-2023
Class II · Moderate risk

Endometrin

cGMP deviations: potential for Microbial Contamination of Non-Sterile Products

Terminated Microbial contamination Ferring Pharmaceuticals Inc NDC 55566-6500-03 D-0879-2023
Class III · Low risk

Lysteda (tranexamic acid)

Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.

Terminated Impurity / degradation Amring Pharmaceuticals Inc NDC 69918-301-30 D-0871-2023

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