AVID Medical, Inc. recalls Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
- Recall date
- November 11, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1001-2026
- FDA classification
- Class I
- Brand / firm
- AVID Medical, Inc.
- Sold / distributed
- US Nationwide distribution in the states of FL, GA and Puerto Rico.
Why it was recalled
Devices are not suitable for organ transplant.
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
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