FDA-Device2024-03-27Class II
Medtronic DLP Vessel Cannula, Model Number REF 30000
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.
Sold states
US and Brazil, Canada, Republic of Georgia, Germany, India, Ireland, Italy, Malaysia, South Africa, UK
Affected count
4343 units
Manufactured in
7611 Northland Dr N, Brooklyn Park, MN, United States
Products
Medtronic DLP Vessel Cannula, Model Number REF 30000
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1316-2024Don't want to check this manually?
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