Somerset Therapeutics recalls methocarbamol injection vials due to bacterial contamination risk in manufacturing. This affects specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
Lack of Assurance of Sterility: Media fill with bacterial contamination
Somerset Therapeutics has recalled methocarbamol injection vials that may contain bacterial contamination. This poses a risk of infection if the medication is used. The recall affects specific lot numbers and expiration dates.
The injection vials were manufactured with a lack of assurance of sterility, meaning they could contain bacterial contamination. This contamination could lead to infections if the medication is administered.
Prescription users of methocarbamol injection vials with specific lot numbers and expiration dates. Patients who have received the recalled vials are at risk of infection.
Check the product label for the lot numbers A240304 to A240391 and expiration dates of 05/2026 or 06/2026. The product is a 10 mL single-dose vial with NDC numbers 70069-101-25 or 70069-101-05.
Look for lot numbers A240304 to A240391 and expiration dates of 05/2026 or 06/2026 on the vial packaging.
The recall indicates a risk of bacterial contamination, so the product should not be used until the manufacturer provides further instructions.
Contact Somerset Therapeutics directly for specific instructions on how to handle the recalled vials.
Check the product label for lot numbers A240304 to A240391 and expiration dates of 05/2026 or 06/2026.
We’ve drafted a message you can send Somerset Therapeutics to request your refund or repair — edit it as you like.
Subject: Recall D-0354-2025 — Somerset Therapeutics Somerset Therapeutics Hello, I own a Somerset Therapeutics that is covered by recall D-0354-2025 from Somerset Therapeutics. 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.
