Medtronic Perfusion Systems recalls EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418
Recalled Product
EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
Hazard / Issue
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Model 77418 UDI-DI: 20763000135618, Lot Numbers: 2022041038; Model 77422 UDI-DI: 20643169485970, Lot Number: 2023020934
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