WhichRecall
Class I — UrgentReported 2026-01-14

Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08

Recalled by AVID Medical, Inc.

Reason for Recall

Devices are not suitable for organ transplant.

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Recall Number
Z-1002-2026
Classification
Class I
Status
Ongoing
Category
device
Initiated
2025-11-11
Reported
2026-01-14
Distribution
US Nationwide distribution in the states of FL, GA and Puerto Rico.
Code Info
Kit Code: JACK097-08; UDI : 10809160462829; Lot No: 1654185.
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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