Asclemed USA recalls lidocaine injections due to lack of sterility assurance. Affected lots may cause infection if used. Contact for return instructions.
Lack of Assurance of Sterility
Asclemed USA recalls certain lidocaine injections because they may not be sterile. Using these could lead to infection, especially in medical procedures.
The injections may not be sterile, which can cause infections if used in medical procedures. This is a risk during procedures where sterile conditions are critical.
Healthcare professionals and patients prescribed this medication. Those using the recalled lots are at risk of infection.
Check for lot numbers AE3102, 031926L01, 032026A01 (expiring 11/30/2026) or AE5052, 052026G01 (expiring 04/30/2028). The product is a 5mL single-dose ampule for prescription use.
Look for lot numbers AE3102, 031926L01, 032026A01 (expiring 11/30/2026) or AE5052, 052026G01 (expiring 04/30/2028) on the ampule.
The recall indicates a lack of sterility assurance, which could lead to infection. Do not use the recalled lots.
Check the lot number on the ampule: AE3102, 031926L01, 032026A01 (expiring 11/30/2026) or AE5052, 052026G01 (expiring 04/30/2028).
The recall does not specify a return process. Contact the manufacturer for guidance.
We’ve drafted a message you can send Asclemed to request your refund or repair — edit it as you like.
Subject: Recall D-0659-2026 — Asclemed Asclemed Hello, I own a Asclemed that is covered by recall D-0659-2026 from Asclemed. 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.
