June 2026 FDA Recall Methohexital Sodium by Onesource Specialty Pharma Limited
D-0662-2026 - Failed Impurities/Degradation Specifications

This Class II drug recall was voluntarily initiated by Onesource Specialty Pharma Limited on June 7, 2026 for the product Methohexital Sodium. The FDA reported the reason for recall as failed impurities/degradation specifications. The product was distributed Nationwide and the recall is currently ongoing.

Recall Number: D-0662-2026

Reason for Recall
Failed Impurities/Degradation Specifications
Initiated
06-07-2026
Reported
07-15-2026
Quantity
4284 vials

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
99220
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Ongoing
Recalling Firm About Recalling Firm
The firm responsible for the recall.
ONESOURCE SPECIALTY PHARMA LIMITED
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States
Product Description About Product Description
Full technical description of the 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

Batch or Lot Expiration Information

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

Affected Packages Involved in this Recall

23155-893-31 Methohexital Sodium