Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Public FDA recall data · checked every hour

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Search 18,003 FDA drug recalls by medication name, or by the NDC code printed on your package.

Popular: Valsartan Metformin Levothyroxine Eye drops

FDA drug recalls on record
18,003
Class I — high risk
1,750
Recalls still ongoing
2,760
Most recent classified recall
Sep 15, 2026
Just announced announced by the firm and posted by FDA; not yet in FDA’s classified recall data

Class I

Latest high-risk recalls

All Class I recalls
Class I · High risk

Dextrose Injection

Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.

Ongoing Particulate / foreign matter Baxter Healthcare Corporation NDC 00338-0719-06 D-0850-2026
Class I · High risk

Epinephrine Injection

Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and glass and broken and leaking vials.

Ongoing Sterility / contamination American Regent, Inc. NDC 0517-3030-01 D-0865-2026

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Unclassified

0.9% Sodium Chloride Injection

Product Mix-up: 0.9% SODIUM CHLORIDE Injection, USP may potentially contain the overwrap with labeling indicating it to be 0.9% SODIUM CHLORIDE Injection, USP but the actual product within the overwrap may be POTASSIUM CHLORIDE Inj.10 mEq

Ongoing Labeling / mix-up Otsuka ICU Medical LLC NDC 0990-7984-23 Recall number pending
Class II · Moderate risk

fentaNYL Citrate

Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product expiry (12/09/2026).

Ongoing Labeling / mix-up OurPharma LLC NDC 73013-1013-01 D-0864-2026
Class II · Moderate risk

Lidocaine Ointment USP

Failed Content Uniformity Specifications. Out of Specification for Assay during analysis at the 24- month long term stability station, at (25¿C,60%RH).

Ongoing Wrong potency / content Sun Pharma /Taro D-0848-2026

Why recalls happen

Most recalls come down to a handful of causes

Every recall in the register is sorted by the reason FDA recorded — contamination, impurities, wrong labels, potency. See which causes are most common and which firms they involve.

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