ONESOURCE SPECIALTY PHARMA LIMITED 2026-07-15 Health serious FDA
Health · FDA · Recall #FDA-D-0662-2026
Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured… Recall
Issued July 15, 2026 · ONESOURCE SPECIALTY PHARMA LIMITED
In July 2026, ONESOURCE SPECIALTY PHARMA LIMITED recalled the Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured…, a serious health recall reported by the FDA.
Compiled by Dana Whitfield, RecallCheckr
What this means for you
Failed Impurities/Degradation Specifications
What you should do
- 1 Stop using Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact ONESOURCE SPECIALTY PHARMA LIMITED to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- ONESOURCE SPECIALTY PHARMA LIMITED
- Category
- Health
- Recall date
- July 15, 2026
- Units affected
- Not reported
- Sold at
- Nationwide within the United States
- Recall number
- FDA-D-0662-2026
- Made in
- India
- Issuing agency
- FDA
In context
- ONESOURCE SPECIALTY PHARMA LIMITED has 1 recall in our database.
- We're tracking 3,673 Health recalls in our database.
- This is the 453rd Health recall we've logged in 2026.