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

354 recalls, newest first

Class I · High risk

PeakMax Capsules

Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.

Ongoing Chemical / undeclared Boulla LLC D-0084-2025
Class I · High risk

VitalityXtra Capsules

Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.

Ongoing Chemical / undeclared Boulla LLC D-0083-2025
Class II · Moderate risk

Xelstrym (dextroamphetamine)

Defective Delivery System: The product does not meet predetermined specifications for Coldflow (adhesive).

Ongoing Packaging defect Noven Pharmaceuticals Inc NDC 68968-0215-3 D-0055-2025
Class III · Low risk

IBU (ibuprofen)

Failed Tablet/Capsule Specifications

Ongoing Failed specification Dr. Reddy's Laboratories, Inc. NDC 55111-683-05 D-0047-2025
Class II · Moderate risk

Timolol Maleate Ophthalmic Solution USP

Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle

Ongoing Packaging defect FDC Limited NDC 64980-514-05 D-0035-2025
Class II · Moderate risk

Cinacalcet Tablets

CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit

Ongoing Nitrosamine impurity Dr. Reddy's Laboratories, Inc. NDC 43598-369-30 D-0028-2025
Class II · Moderate risk

Cinacalcet Tablets

CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit

Ongoing Nitrosamine impurity Dr. Reddy's Laboratories, Inc. NDC 43598-368-30 D-0027-2025
Class II · Moderate risk

Cinacalcet Tablets

CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit

Ongoing Nitrosamine impurity Dr. Reddy's Laboratories, Inc. NDC 43598-367-30 D-0026-2025
Class II · Moderate risk

Liceout

CGMP violations.

Ongoing cGMP deviation Neogen Corporation D-0074-2025

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