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Medtronic Perfusion Systems recalls Medtronic Vessel Cannulae: a) DLP¿ 2 mm Vessel Cannula Blunt Tip, Model Number 30004; b) DLP¿ 3 mm Vessel Cannula
Recalled May 22, 2024 · FDA recall Z-1799-2024 · Medtronic Perfusion Systems
Hazard
Potential for unsealed sterile packing. · FDA Class II
Units
5719 units
Sold at
Worldwide distribution.
Description
Potential for unsealed sterile packing.
Product
Medtronic Vessel Cannulae: a) DLP¿ 2 mm Vessel Cannula Blunt Tip, Model Number 30004; b) DLP¿ 3 mm Vessel Cannula Blunt Tip, Model Number 30003
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →