FDA recall Z-1796-2024
Medtronic Perfusion Systems · Class II · device
Product
Medtronic I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001
Reason for recall
Potential for unsealed sterile packing.
Distribution
Worldwide distribution.
Key facts
- Status
- Ongoing
- Initiation date
- 2024-03-19
- Report date
- 2024-05-22
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Brooklyn Park, MN, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1796-2024