Class II

Medical Device Recall: DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 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

745 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0984-2025

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.

Medtronic Perfusion Systems Medical Device Recall: DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr) | SafeCheck