Onesource Specialty Pharma Limited: Methohexital Sodium For Injection, Usp 500 Mg Multiple Dose Vial
Recall Summary OneSource Specialty Pharma is recalling Methohexital Sodium for Injection 500 mg multiple-dose vials (NDC 23155-893-31) distributed nationwide because the product failed to meet purity standards—it contains higher levels of impurities or degradation products than allowed. This is a Class II recall, meaning the product could cause serious health problems. The affected medication was manufactured in India for Avet Pharmaceuticals and distributed across all U.S. states and Washington, D.C.
- Recalling firm
- ONESOURCE SPECIALTY PHARMA LIMITED
- Product
- 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
- Reason
- Failed Impurities/Degradation Specifications
- Classification
- Class II
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-06-07
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Nationwide within the United States
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/18610694-fb61-40d2-b3ad-7d8b2c1261ad