FDA recall Z-1002-2026
AVID Medical, Inc. · Class I · device
Product
Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
Reason for recall
Devices are not suitable for organ transplant.
Distribution
US Nationwide distribution in the states of FL, GA and Puerto Rico.
Key facts
- Status
- Ongoing
- Initiation date
- 2025-11-11
- Report date
- 2026-01-14
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Toano, VA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1002-2026