United StatesMethohexital Sodium for Injection, USP 500 mg multiple-dose vial (NDC 23155-893-31), Lot #7000612A, Exp. 1/2028, manufactured by OneSource Specialty Pharma Limited for Avet Pharmaceuticals, is affected. The firm is recalling 4,284 vials distributed nationwide in the United States after the product failed impurities/degradation specifications.
What's being 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
Recalling firm: Onesource Specialty Pharma Limited, Bengaluru, N/A, India.
How to identify it
Lot #: 7000612A, Exp. Date 1/2028
The hazard
Failed Impurities/Degradation Specifications
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Nationwide within the United States
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)