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.
Failed Impurities/Degradation Specifications
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.
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.
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.
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.
Look for the lot number 7000612A and expiration date 1/2028 on the vial label.
The recall indicates potential impurities that could cause serious injury, so it is not safe to use without consulting a healthcare provider.
The recall does not specify a remedy, so contact your healthcare provider for guidance on safe handling.
Check for the lot number 7000612A and expiration date 1/2028 on the vial label.
We’ve drafted a message you can send OneSource Specialty Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0662-2026 — OneSource Specialty Pharma OneSource Specialty Pharma Hello, I own a OneSource Specialty Pharma that is covered by recall D-0662-2026 from OneSource Specialty Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
