AVID Medical recalls HVI CARDIAC ROBOT PACK medical kits due to discoloration from resterilization. Affected kits may have visual issues but no injury risk.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
AVID Medical is recalling HVI CARDIAC ROBOT PACK medical kits because resterilization caused discoloration. This issue doesn't 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 HVI CARDIAC ROBOT PACK kits are likely affected. Those with kits from Lot No. 1625487 are at most risk.
Check for the model number RYCB72-04 on the kit. Kits with Lot No. 1625487 were affected by the resterilization issue.
Review the model number and lot number on the kit to confirm if it is affected.
No, the discoloration is a cosmetic issue and does not pose a safety risk.
Check the model number and lot number to see if it is affected; no action is needed if it's not.
Kits with model number RYCB72-04 and lot number 1625487 were affected by the resterilization issue.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2252-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2252-2025 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.
