AVID Medical recalls Halyard Transport Bag Kit (Kit Code LIFE0080-01) due to potential sterility compromise. Affected units may not maintain sterile conditions during medical procedures.
Tyvek bag seal issue which may compromise sterility of the kit.
AVID Medical is recalling their Halyard Transport Bag Kit (Kit Code LIFE0080-01) because the Tyvek bag seal might not stay sterile. This could lead to infections during medical procedures if the kit isn't properly sealed.
The Tyvek bag seal may not stay properly sealed, which could allow contamination. This might compromise the sterility of the kit during medical procedures, increasing infection risk.
Healthcare professionals using the kit for medical procedures are most at risk. Patients receiving care with this kit could be affected if sterility is compromised.
Check for Kit Code LIFE0080-01 on the product. The product was sold with UDI-DI: 10809160314500 and Lot Number 1650056, expiring July 24, 2028.
Verify the Kit Code is LIFE0080-01 and the Lot Number is 1650056.
The recall indicates a potential sterility risk, so it's not recommended for use until the issue is resolved.
Check for Kit Code LIFE0080-01, Lot Number 1650056, and UDI-DI: 10809160314500 on the product.
The recall does not specify a remedy, so contact AVID Medical for guidance.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1338-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-1338-2026 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.
