ONESOURCE SPECIALTY PHARMA LIMITED recalls Methohexital Sodium for Injection
- Recalling company
- 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 – may cause temporary or medically reversible health consequences
- Recall date
- Jun 7, 2026
- Reported
- Jul 15, 2026
- Distribution
- Nationwide within the United States
- Status
- Ongoing
- Quantity
- 4284 vials
- Lot / codes
- Lot #: 7000612A, Exp. Date 1/2028
- Company location
- Bengaluru, N/A
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0662-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0662-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.