Huons Co. recalls Bupivacaine Hydrochloride 0.75% in 8.25% Dextrose Injection ampules due to lack of sterility assurance. This affects prescription-only products sold in the US with specific NDC numbers.
Lack of Assurance of Sterility
Huons Co. is recalling prescription bupivacaine injections because they may not be sterile. This could lead to infections if used improperly. The recall affects specific ampule sizes and quantities sold in the US.
The product lacks assurance of sterility, meaning it could contain harmful bacteria or other contaminants. If used for medical procedures, this could cause serious infections or other health issues.
Prescription users of this bupivacaine injection product in the US. Healthcare professionals and patients who received the recalled ampules are most at risk.
Check for NDC numbers 73293-0002-1 (2 mL ampule) or 73293-0002-2 (50 x 2 single-dose ampules). The product is prescription-only and sold in the US with specific packaging.
Verify the NDC numbers and product size to confirm if it's part of the recall.
The recall indicates a lack of sterility assurance, so it is not safe to use. The product should be discarded or returned.
The affected NDC numbers are 73293-0002-1 (2 mL ampule) and 73293-0002-2 (50 x 2 single-dose ampules).
The recall record does not specify a replacement option or remedy.
We’ve drafted a message you can send Huons Co. to request your refund or repair — edit it as you like.
Subject: Recall D-0530-2026 — Huons Co. Huons Co. Hello, I own a Huons Co. that is covered by recall D-0530-2026 from Huons Co.. 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.
