[Recalled] Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17. — Devices are not suitable for organ transplant | FDA 2025-11-11
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17. |
|---|---|
| Brand / manufacturer | AVID Medical, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1001-2026 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 11 November 2025 |
| EAN / barcode | 10809160460726 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Devices are not suitable for organ transplant.
This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
Related recalls from AVID Medical, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.