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Medtronic Perfusion Systems recalls Medtronic I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001
Recalled May 22, 2024 · FDA recall Z-1796-2024 · Medtronic Perfusion Systems
Hazard
Potential for unsealed sterile packing. · FDA Class II
Units
7935 units
Sold at
Worldwide distribution.
Description
Potential for unsealed sterile packing.
Product
Medtronic I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →