AVID Medical recalls GYN ROBOTIC PACK kits due to discoloration from resterilization. Affected kits have specific model and lot numbers. No action is required as the hazard is cosmetic.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
AVID Medical is recalling GYN ROBOTIC PACK medical kits because discoloration occurred during resterilization. This issue does not pose a safety risk but may affect appearance. No action is needed as the problem is cosmetic.
The CLEARIFY VISUALIZATION SYSTEM in the kits was inadvertently resterilized, causing discoloration. This discoloration is a cosmetic issue and does not affect the functionality or safety of the product.
Medical professionals using the GYN ROBOTIC PACK kits with model NAMC474-01 and specific lot numbers are affected. The risk is minimal as the discoloration is cosmetic and not a safety hazard.
Check for model number NAMC474-01 and lot numbers 1620573, 1620572, 1621883, 1621884, or 1628673 on the kit packaging or label.
Inspect the kit for discoloration, which is a cosmetic issue not affecting safety.
No action is required as the discoloration is cosmetic and does not pose a safety risk.
Model NAMC474-01 with lot numbers 1620573, 1620572, 1621883, 1621884, and 1628673.
No, the discoloration is cosmetic and does not affect the product's safety or functionality.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2251-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2251-2025 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.
