Class II

Medical Device Recall: EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)

Medtronic Perfusion Systems · December 12, 2024

Reason for Recall

Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.

Distribution

Worldwide - US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

930 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0985-2025

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.