AVID Medical recalls DAVINCI TRUCUSTOM BUNDLE kits with discoloration due to resterilization. Affected models include MAMC228-13 to MAMC228-15. No action needed as discoloration is cosmetic.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
AVID Medical is recalling DAVINCI TRUCUSTOM BUNDLE medical convenience kits that may have discoloration from resterilization. This issue does not affect safety or function but could impact appearance.
The CLEARIFY VISUALIZATION SYSTEM in the kits was resterilized incorrectly, causing discoloration. This issue does not affect the device's safety or functionality but may alter its appearance.
Medical professionals using the DAVINCI TRUCUSTOM BUNDLE kits with model numbers MAMC228-13 through MAMC228-15. Patients or staff using these kits are at minimal risk due to the cosmetic nature of the discoloration.
Check for model numbers MAMC228-13, MAMC228-14, or MAMC228-15 on the kit. The UDI codes listed in the recall notice also help identify affected units.
Inspect the kit for discoloration, which is a cosmetic issue but may be visible.
No, the discoloration is cosmetic and does not affect safety or function.
No action is required as the discoloration is not a safety hazard.
Model numbers MAMC228-13, MAMC228-14, and MAMC228-15.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2244-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2244-2025 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.
