Medtronic DLP Vessel Cannula, Model Number REF 30000
- Company
- Medtronic Perfusion Systems
- Recall Initiated
- February 7, 2024
- Posted
- March 19, 2024
- Recall Number
- Z-1316-2024
- Quantity
- 4343 units
- Firm Location
- Brooklyn Park, MN
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
Lot / Code Info
UDI/DI 20613994646211, Lot Numbers: 2023020890, 202305C126, 2023020889
Root Cause
Packaging change control
Action Taken
Medtronic Cardiac Surgery issued an Urgent: Medical Device Recall to its consignees on 02/07/2024 via UPS. The notice explained the issue, potential risk, and requested consignees identify and quarantine affected product, and arrange to return the affected product by contacting customer service at 1-800-854-3570, option 1, then Option 4. The notification should be shared with others in your organization as appropriate. If product was forwarded to another facility, please notify the facility of this Medtronic Urgent Medical Device Recall.