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Medtronic Perfusion Systems recalls Extra corporeal circuit with bio-active surface.
Recalled July 15, 2020 · FDA recall Z-2495-2020 · Medtronic Perfusion Systems
Hazard
Affected products failed a sterilization test. · FDA Class II
Units
10 units
Sold at
Domestic Distribution only to CA and MI.
Description
Affected products failed a sterilization test.
Product
Extra corporeal circuit with bio-active surface.
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →