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Medtronic Perfusion Systems recalls Medtronic Aortic Root Cannulae and Cardioplegia Needles: a) DLP¿ 9 Ga (11 Fr) Aortic Root Cannula, Model Number 24009
Recalled May 22, 2024 · FDA recall Z-1800-2024 · Medtronic Perfusion Systems
Hazard
Potential for unsealed sterile packing. · FDA Class II
Units
2622 units
Sold at
Worldwide distribution.
Description
Potential for unsealed sterile packing.
Product
Medtronic Aortic Root Cannulae and Cardioplegia Needles: a) DLP¿ 9 Ga (11 Fr) Aortic Root Cannula, Model Number 24009; b) DLP¿ 16 Ga (5 Fr) Cardioplegia Needle Neonatal 0.64 cm (1/4 in) Tip Length, Model Number 11316; c) M+AR" 14 Ga (7 Fr) Aortic Root Cannula with Flow-Guard", Model Number 11014L
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →