Class II

Drug Recall: 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.

ONESOURCE SPECIALTY PHARMA LIMITED · June 7, 2026

Reason for Recall

Failed Impurities/Degradation Specifications

Product Description

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

Distribution

Nationwide within the United States

States Affected

NATIONWIDE

Quantity Affected

4284 vials

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0662-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

ONESOURCE SPECIALTY PHARMA LIMITED Drug Recall: 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. | SafeCheck