AVID Medical recalls Pack General Robotic medical kits due to discoloration from resterilization. Affected kits have specific model numbers and lot codes. No action needed for safety.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
AVID Medical is recalling Pack General Robotic medical convenience kits because discoloration occurred during resterilization. This issue does not pose a safety risk but may affect appearance.
The CLEARIFY VISUALIZATION SYSTEM in the kits was resterilized incorrectly, causing discoloration. This is a cosmetic issue that does not affect safety or function.
Medical professionals using the Pack General Robotic kits are likely affected. Those with the specific model numbers and lot codes listed are most at risk.
Check for model number RDLD047-10 and lot numbers 1589630, 1590570, 1610157, 1617028, 1618142, 1621537, 1629589, 1635288, or 1636852 on the kit packaging.
Verify the model number and lot numbers listed in the recall notice to confirm if your kit is affected.
No, the discoloration is a cosmetic issue and does not pose a safety risk.
No action is required as the discoloration does not affect safety or function.
Model number RDLD047-10 with lot numbers 1589630, 1590570, 1610157, 1617028, 1618142, 1621537, 1629589, 1635288, or 1636852.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2259-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2259-2025 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.
