Medical device recalls High risk

AVID Medical, Inc. recalls Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.

Recall date
November 11, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1000-2026
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: LLOG1000-15.

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