AVID Medical recalls specific General Robotic Packs due to discoloration from resterilization. Affected kits may have visual issues but pose no safety risk. Contact for details.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
AVID Medical is recalling certain General Robotic Packs that may show discoloration after resterilization. This issue does not affect safety but could impact appearance.
The CLEARIFY VISUALIZATION SYSTEM in the kits was resterilized incorrectly, causing discoloration. This is a cosmetic issue and does not pose a safety hazard.
Medical professionals using the General Robotic Packs for convenience. Those with the specific model numbers listed are most affected.
Check for model numbers NAFB082-04 or NAMC473-01 on the kit. Look for lot numbers 1568211 through 1635911 in the product description.
Verify the model number and lot number against the list provided in the recall notice.
No, the discoloration is cosmetic and does not pose a safety risk.
Check the model and lot numbers against the list provided. No action is needed if the product is safe.
Look for model numbers NAFB082-04 or NAMC473-01 and lot numbers from the list provided 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-2248-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2248-2025 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.
