Medtronic DLP Vessel Cannula recall: Labeling Error
Medtronic DLP Vessel Cannula, Model Number REF 30000
Why was Medtronic DLP Vessel Cannula 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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI 20613994646211, Lot Numbers: 2023020890, 202305C126, 2023020889
- Product
- Medtronic DLP Vessel Cannula, Model Number REF 30000
- Recalling firm
- Medtronic Perfusion Systems
- Quantity
- 4343 units
- Distribution
- US and Brazil, Canada, Republic of Georgia, Germany, India, Ireland, Italy, Malaysia, South Africa, UK
- Recall date
- March 27, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)