AVID Medical recalls CT DAVINCI medical convenience kits with discoloration due to resterilization. Affected kits may have visual issues; contact for details.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
AVID Medical is recalling CT DAVIN: Medical convenience kits that may have discoloration from improper resterilization. This could affect visual accuracy during medical procedures.
The visualization system in the kit was resterilized incorrectly, causing discoloration. This may affect visual accuracy during medical procedures but does not pose a direct safety risk.
Medical professionals using the CT DAVINCI convenience kits are most at risk. The recall applies to kits sold with specific model and lot numbers.
Check for model number WRNM089 and lot number 1627141 on the kit. The kit also has a unique device identifier (UDI) 10809160432525.
Look for model number WRNM089 and lot number 1627141 on the kit.
The visualization system was inadvertently resterilized, causing discoloration that may affect visual accuracy during medical procedures.
Check for model number WRNM089 and lot number 1627141. Contact AVID Medical for further instructions.
The discoloration does not pose a direct safety risk but may affect visual accuracy during medical procedures.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2242-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2242-2025 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.
