FDA recall Z-2407-2026
AVID Medical, Inc. · Class II · device
Product
Halyard, Pain Pack. Kit Code: AMPK48-01.
Reason for recall
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Distribution
US Nationwide distribution in the state of Iowa.
Key facts
- Status
- Ongoing
- Initiation date
- 2026-04-30
- Report date
- 2026-06-17
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Toano, VA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2407-2026