AVID Medical recalls LAVH Pack medical kits with discoloration due to resterilization. Affected kits have specific model numbers and lot numbers. Consumers should check their kit details to determine if recalled.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
AVID Medical is recalling certain LAVH Pack medical convenience kits because resterilization caused discoloration. This issue does not pose a safety risk but may affect the kit's appearance and functionality.
The CLEARIFY VISUALIZATION SYSTEM in the kits was resterilized incorrectly, leading to discoloration. This discoloration does not cause injury but may indicate a problem with the kit's appearance or internal components.
Medical professionals using the LAVH Pack kits with model numbers USAR053-11 and specific lot numbers listed in the recall. Those who use these kits for medical procedures are most at risk of noticing discoloration.
Check for model number USAR053-11 and lot numbers 1578109, 1585712, 1597106, 1601742, 1601643, 1607925, 1612044, 1621429, or 1637117 on the kit's packaging or label.
Look for model number USAR053-11 and specific lot numbers listed in the recall to confirm if your kit is affected.
No, the discoloration does not cause injury or health risks. It is a cosmetic issue related to resterilization.
Check for model number USAR053-11 and lot numbers 1578109, 1585712, 1597106, 1601742, 1601643, 1607925, 1612044, 1621429, or 1637117 on the kit's packaging.
The recall does not require action beyond checking if your kit is affected. There is no remedy specified 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-2257-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2257-2025 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.
