AVID Medical recalls Halyard Organ Recovery Pack (Kit Code LLOG1000-15) due to being unsuitable for organ transplant. Affected units have specific lot numbers and UDI.
Devices are not suitable for organ transplant.
AVID Medical is recalling their Haly: Organ Recovery Pack (Kit Code LLOG1000-15) because it is not designed for organ transplant use. This could lead to improper medical procedures if used incorrectly.
The device is not suitable for organ transplant procedures, which could lead to improper handling or failure during the transplant process. This poses a risk to patient safety and medical outcomes.
People who own or use the Halyard Organ Recovery Pack with Kit Code LLOG1000-15 are affected. Medical professionals handling organ transplants are most at risk.
Check for Kit Code LLOG1000-15 on the product. Affected units have specific lot numbers: 1632138 and 1648393, and a unique device identifier (UDI) of 10809160432679.
Look for Kit Code LLOG1000-15, lot numbers 1632138 or 1648393, and UDI 10809160432679 on the device.
No, the device is not suitable for organ transplant use as stated in the recall.
The recall does not specify a remedy, so check the product details to confirm if it is affected and contact AVID Medical for further guidance.
Check for Kit Code LLOG1000-15, lot numbers 1632138 or 1648393, and UDI 10809160432679 on the device.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1000-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-1000-2026 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.
