Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1001-2026 — Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.

U.S. FDA — Device Enforcement · United States · 2025-11-11 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1001-2026
Date of alert: 2025-11-11
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: AVID Medical, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10809160460726

Reported risk: Devices are not suitable for organ transplant.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-1001-2026 — Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.

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