AVID Medical recalls specific LAPAROSCOPY PACK kits due to discoloration from resterilization. Affected kits have model numbers VAML025-05 and WRNM007-15. No action is required as the issue is cosmetic.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
AVID Medical is recalling certain LAPAROSCOPY PACK medical kits because they were resterilized incorrectly, causing discoloration. This issue does not pose a safety risk and does not require action from users.
The CLEARIFY VISUALIZATION SYSTEM in the kits was resterilized incorrectly, leading to discoloration. This discoloration is a cosmetic issue and does not affect the functionality or safety of the kit.
Medical professionals using the recalled LAPAROSCOPY PACK kits for procedures. The risk is minimal as the discoloration is cosmetic and not a safety hazard.
Check for model numbers VAML025-05 or WRNM007-15 on the kit. The kits were sold with lot numbers including 1580078 through 1639643.
Inspect the kit for discoloration, which is a cosmetic issue and not a safety hazard.
No action is required as the discoloration is cosmetic and does not affect safety.
Model numbers VAML025-05 and WRNM007-15 are affected.
Check for model numbers VAML025-05 or WRNM007-15 and lot numbers listed in the recall notice.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2256-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2256-2025 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.
