Class II

Medical Device Recall: Medtronic I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001

Medtronic Perfusion Systems · March 19, 2024

Reason for Recall

Potential for unsealed sterile packing.

Distribution

Worldwide distribution.

Quantity Affected

7935 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1796-2024

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.

Medtronic Perfusion Systems Medical Device Recall: Medtronic I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001 | SafeCheck