FDA recall Z-0986-2025
Medtronic Perfusion Systems · Class II · device
Product
Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
Reason for recall
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Distribution
Worldwide - US Nationwide distribution.
Key facts
- Status
- Ongoing
- Initiation date
- 2024-12-12
- Report date
- 2025-01-29
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Brooklyn Park, MN, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0986-2025