Reported Mar 27, 2024 · Ongoing
Medtronic DLP Vessel Cannula, Model Number REF 30000
Medtronic Perfusion Systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Perfusion Systems · 7611 Northland Dr N · Brooklyn Park, MN · 55428-1088
Is this the product you have?
- Medtronic DLP Vessel Cannula, Model Number REF 30000
- Lot codes and dates
- UDI/DI 20613994646211
- Lot Numbers
2023020890202305C1262023020889
- Amount recalled
- 4343 units
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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