FDAFDA · Food and drugs·Recall number Z-1316-2024
Medtronic DLP Vessel Cannula, Model Number REF 30000
Published March 27, 2024 · Recall initiated: February 7, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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 to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Medtronic Perfusion Systems
- Distributor
- US and Brazil, Canada, Republic of Georgia, Germany, India, Ireland, Italy, Malaysia, South Africa, UK
- Lot
- UDI/DI 20613994646211, Lot Numbers: 2023020890, 202305C126, 2023020889
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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