Class II

Medical Device Recall: Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312

Medtronic Perfusion Systems · July 9, 2024

Reason for Recall

During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).

Distribution

Worldwide distribution - US Nationwide and the countries of Cambodia, Greece, Ireland, Italy, Saudi Arabia, Switzerland, United Kingdom, Viet Nam.

States Affected

NATIONWIDE

Quantity Affected

290 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3128-2024

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 DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312 | SafeCheck