OneSource Specialty Pharma Methohexital Sodium Recall: Impurities Risk Serious Injury
OneSource Specialty Pharma recalls Methohexital Sodium 500mg vials due to impurities that could cause serious injury during medical use. Affected vials have specific lot numbers and expiration dates.
Use caution until it’s fixed
Failed Impurities/Degradation Specifications
Contact the company
What happened, in plain English
OneSource Specialty Pharma is recalling Methohexital Sodium for Injection vials because they may contain impurities that could cause serious injury if used improperly. This is a medication for medical use only, so patients should not use the recalled vials without consulting their healthcare provider. Read more at govinfonow.com/recall/31215-onesource-specialty-pharma-methohexital-sodium-recall-impurities-risk-serious-injury.
Source Summary by GovInfoNow · govinfonow.com/recall/31215-onesource-specialty-pharma-methohexital-sodium-recall-impurities-risk-serious-injury · Updated August 10, 2026 · FDA enforcement record: FDA #D-0662-2026
Cite this page
“OneSource Specialty Pharma Methohexital Sodium Recall: Impurities Risk Serious Injury.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/31215-onesource-specialty-pharma-methohexital-sodium-recall-impurities-risk-serious-injury. Based on FDA recall #D-0662-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0662-2026%22&limit=1).
Why it’s dangerous
The vials may contain impurities that could cause serious injury during medical use. This is a medication for injection only, so improper use could lead to adverse effects.
Who’s affected
Healthcare professionals who use this medication for medical procedures. Patients receiving this drug under a prescription are at risk if they use the recalled vials.
How to tell if you have this one
Check for the product name 'Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only'. The lot number 7000612A and expiration date 1/2028 are specific to this recall.
- Brand
OneSource Specialty Pharma- Category
Drug
What to do — step by step
Check Product Details
Look for the lot number 7000612A and expiration date 1/2028 on the vial label.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide within the United States” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 38 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0662-2026 (June 7, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0662-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.