Medtronic DLP Vessel Cannula, Model Number REF 30000
Reported: March 27, 2024 Initiated: February 7, 2024 #Z-1316-2024
Product Description
Medtronic DLP Vessel Cannula, Model Number REF 30000
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.
Details
- Recalling Firm
- Medtronic Perfusion Systems
- Units Affected
- 4343 units
- Distribution
- US and Brazil, Canada, Republic of Georgia, Germany, India, Ireland, Italy, Malaysia, South Africa, UK
- Location
- Brooklyn Park, MN
Frequently Asked Questions
What product was recalled? ▼
Medtronic DLP Vessel Cannula, Model Number REF 30000. Recalled by Medtronic Perfusion Systems. Units affected: 4343 units.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 27, 2024. Severity: Moderate. Recall number: Z-1316-2024.
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