Official recall notice

FDA DrugClass IINotable

Methohexital Sodium for Injection Recall (Jul 2026)

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

Recall date
2026-07-15
Category
Drug
FDA class
Class II

Why it was recalled

Hazard

Failed Impurities/Degradation Specifications

One email a week when there are new recalls. Confirm by email; unsubscribe anytime.

Product description

Failed Impurities/Degradation Specifications

Affected products

Lot #: 7000612A, Exp. Date 1/2028

Verify with the official notice →
Share:

Related Recalls

2026-10-21 · FDA_DRUG
FDA Recall: No Brand Name: Compounded veterinary medications
No Brand Name
2026-10-14 · FDA_DRUG
FDA Recall: Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/60, injectable, Packaged in single-use dosage syringes, total mL
Carolina Infusion, LLC
2026-10-14 · FDA_DRUG
FDA Recall: Sterile Lubricant Dry Eye Relief Eye Drops, 0.5 FL OZ (15 mL); a) LEADER, DISTRIBUTED BY CARDINAL HE
K.C. Pharmaceuticals, Inc.
2026-10-14 · FDA_DRUG
FDA Recall: Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/10, injectable, Packaged in single-use dosage syringes, total mL
Carolina Infusion, LLC