Recall archive / FDA device enforcement
Medtronic DLP Vessel Cannula, Model Number REF 30000 — FDA record Z-1316-2024
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Feb 7, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Medtronic DLP Vessel Cannula, Model Number REF 30000
- Reason
- 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.
- Classification
- Class II
- Recalling firm
- Medtronic Perfusion Systems
- Quantity
- 4343 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1316-2024
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI/DI 20613994646211, Lot Numbers: 2023020890, 202305C126, 2023020889 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US and Brazil, Canada, Republic of Georgia, Germany, India, Ireland, Italy, Malaysia, South Africa, UK
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Mar 27, 2024
- Recall initiation date
- Feb 7, 2024
- Center classification date
- Mar 19, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.