AVID Medical recalls partial nephrectomy packs due to discoloration from resterilization. Affected kits have specific model numbers and lot codes. Consumers should contact for details.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
AVID Medical is recalling partial nephrectomy packs that may have discoloration due to resterilization. This issue does not pose a safety risk but could affect the kit's appearance and functionality.
The CLEARIFY VISUALIZATION SYSTEM in the kits was resterilized incorrectly, causing discoloration. This does not cause injury or malfunction but may affect the kit's visual appearance.
Surgical teams and medical professionals using the recalled nephrectomy packs. The risk is minimal as discoloration does not impact safety.
Check for model numbers NAMC077 or NAMC077-02 and lot numbers 1591073, 1612261, 1616916, 1632036, 1632038, or 1632359. The kits were sold with specific UDI codes.
Verify model numbers and lot numbers to confirm if your kit is affected.
No, discoloration does not cause injury or malfunction but may affect appearance.
Check for model numbers NAMC077 or NAMC077-02 and lot numbers 1591073, 1612261, 1616916, 1632036, 1632038, or 1632359.
Contact AVID Medical for details on next steps.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2261-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2261-2025 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.
