FDA · Drugs ·
Methohexital Sodium for Injection recall
ONESOURCE SPECIALTY PHARMA LIMITED recalled Methohexital Sodium for Injection on July 15, 2026 because of failed Impurities/Degradation Specifications. It was sold nationwide.
Why it was recalled
Failed Impurities/Degradation Specifications
What's 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
Quantity: 4284 vials
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- ONESOURCE SPECIALTY PHARMA LIMITED, Bengaluru, N/A
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
Nationwide within the United States - Status
- Ongoing
- Recall number
- D-0662-2026
- Source
- U.S. Food and Drug Administration
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