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.