Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA drug recalls in 2024

Every FDA drug recall initiated in 2024, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.

557 recalls, newest first.

Class II · Moderate risk

S.P.Labs

Failed Stability Specifications

Completed Stability / shelf life Specialty Process Labs LLC NDC 81305-500-01 D-0446-2024
Class II · Moderate risk

FentaNYL citrate

Lack of Assurance of Sterility: Firm did not perform process validation.

Ongoing Sterility / contamination SSM Health Care St. Louis DBA SSM St. Clare Health Center D-0436-2024
Class II · Moderate risk

Phenylephrine HCl

Lack of Assurance of Sterility: Firm did not perform process validation.

Ongoing Sterility / contamination SSM Health Care St. Louis DBA SSM St. Clare Health Center D-0435-2024
Class II · Moderate risk

Tobramycin for Injection

Failed Stability Specification: Water determination was found not complying with specification.

Terminated Stability / shelf life Eugia US LLC NDC 55150-470-06 D-0385-2024
Class III · Low risk

Clindamycin Phosphate

Defective Container: Out of specification for weight due to a slow leakage at the 12-month stability timepoint.

Ongoing Packaging defect Contract Pharmaceuticals Limited Canada NDC 10135-0691-61 D-0364-2024
Class II · Moderate risk

Lidocaine HCL 1%

Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.

Ongoing Particulate / foreign matter Denver Solutions, LLC DBA Leiters Health NDC 71449-090-42 D-0363-2024
Class II · Moderate risk

Moxifloxacin 5mg/ml

Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.

Ongoing Particulate / foreign matter Denver Solutions, LLC DBA Leiters Health NDC 71449-097-42 D-0362-2024
Class II · Moderate risk

Moxifloxacin PF

Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.

Ongoing Particulate / foreign matter Denver Solutions, LLC DBA Leiters Health NDC 71449-096-42 D-0361-2024
Class II · Moderate risk

PROBLEND Hand Sanitizer

CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.

Terminated cGMP deviation Seatex LLC D-0360-2024
Class II · Moderate risk

7 Eleven Hand Sanitizer Gel

CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.

Terminated cGMP deviation Seatex LLC D-0359-2024

Recalls by year