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Medtronic Perfusion Systems recalls Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
Recalled May 22, 2024 · FDA recall Z-1795-2024 · Medtronic Perfusion Systems
Hazard
Potential for unsealed sterile packing. · FDA Class II
Units
250 units
Sold at
Worldwide distribution.
Description
Potential for unsealed sterile packing.
Product
Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →