Medtronic Perfusion Systems: Medical Device Recall in 2024 - (Recall #: Z-1316-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Medtronic DLP Vessel Cannula, Model Number REF 30000

Product Classification:

Class II

Date Initiated: February 7, 2024

Date Posted: March 27, 2024

Recall Number: Z-1316-2024

Event ID: 94068

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.

Status: Ongoing

Product Quantity: 4343 units

Code Information:

UDI/DI 20613994646211, Lot Numbers: 2023020890, 202305C126, 2023020889

Distribution Pattern:

US and Brazil, Canada, Republic of Georgia, Germany, India, Ireland, Italy, Malaysia, South Africa, UK

Voluntary or Mandated:

Voluntary: Firm initiated