Class II
Medical Device Recall: 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
Medtronic Perfusion Systems · March 19, 2024
Reason for Recall
Potential for unsealed sterile packing.
Distribution
Worldwide distribution.
Quantity Affected
5719 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1799-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.