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Medtronic Perfusion Systems recalls Medtronic DLP Vessel Cannula, Model Number REF 30000
Recalled March 27, 2024 · FDA recall Z-1316-2024 · Medtronic Perfusion Systems
Hazard
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. · FDA Class II
Units
4343 units
Sold at
US and Brazil, Canada, Republic of Georgia, Germany, India, Ireland, Italy, Malaysia, South Africa, UK
Description
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.
Product
Medtronic DLP Vessel Cannula, Model Number REF 30000
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →