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Class II · ModerateActive recall

Methohexital Sodium

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: 7000612A, Exp. Date 1/2028
Where it was soldNationwide within the United States
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Failed Impurities/Degradation Specifications

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byOneSource Specialty, Pharma Limited, Bengaluru - 561 203, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816 foreign manufacturer
Brand nameMETHOHEXITAL SODIUM
Generic nameMETHOHEXITAL SODIUM
Active ingredient(s)METHOHEXITAL SODIUM
Distributed by / forAvet Pharmaceuticals Inc., East Brunswick, NJ 08816
NDC23155-893-31
Show the full FDA record
Full product labelMethohexital 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 firmONESOURCE SPECIALTY PHARMA LIMITED
DistributionNationwide within the United States
Quantity4284 vials
Recall initiated2026-06-07
Report date2026-07-15
Recall completed—
Recall numberD-0662-2026
ClassificationClass II
FDA statusOngoing
Origin on fileBengaluru N/A India

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.