US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jun 7, 2026 (3 months ago)

Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Impurities/Degradation Specifications

What was recalled

Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured by: OneSource Specialty, Pharma Limited, Bengaluru - 561 203, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-893-31

Recalling firm
Onesource Specialty Pharma Limited
NDC code
23155-893-31
Origin
N/A, India
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0662-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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