AVID Medical recalls LAPAROSCOPIC GYN. Medical convenience kits with discoloration due to resterilization. Affected kits may have cosmetic issues but no safety risk.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
AVID Medical is recalling LAPAROSCOPIC GYN. Medical convenience kits that were resterilized, causing discoloration. This is a cosmetic issue with no safety risk.
The kits were resterilized incorrectly, leading to discoloration. This is a cosmetic issue that does not affect safety or functionality.
Medical professionals using the LAPAROSCOPIC GYN. Medical convenience kits. The risk is minimal as this is a cosmetic issue with no safety implications.
Check for Model No. EURO011-08 and Kit Lot No. 1613056. The kits were sold with UDI: 10809160414248.
Identify the model number (EURO011-08) and lot number (1613056) to confirm if the kit is affected.
No, this recall is for cosmetic discoloration only and does not pose a safety risk.
Check the model number and lot number to see if it matches the affected kits. No action is needed if it's not affected.
Look for Model No. EURO011-08 and Kit Lot No. 1613056. The kits were sold with UDI: 10809160414248.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2254-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2254-2025 from AVID Medical. 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.
