Home / Recalls / Medical Devices
Medtronic Perfusion Systems recalls Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
Recalled January 29, 2025 · FDA recall Z-0986-2025 · Medtronic Perfusion Systems
Hazard
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae. · FDA Class II
Units
440 units
Sold at
Worldwide - US Nationwide distribution.
Description
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Product
Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →