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Medtronic Perfusion Systems recalls EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
Recalled January 29, 2025 · FDA recall Z-0985-2025 · Medtronic Perfusion Systems
Hazard
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae. · FDA Class II
Units
930 units
Sold at
Worldwide - US Nationwide distribution.
Description
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Product
EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →