Class II
Medical Device Recall: Medtronic DLP Vessel Cannula, Model Number REF 30000
Medtronic Perfusion Systems · February 7, 2024
Reason for Recall
Medtronic is writing to inform you of incorrect labeling for three manufactured lots of the DLP Vessel Cannulae for the model and lot numbers listed above.
Distribution
US and Brazil, Canada, Republic of Georgia, Germany, India, Ireland, Italy, Malaysia, South Africa, UK
Quantity Affected
4343 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1316-2024
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.