FDA-Device2025-09-10Class I
DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT 10FR, Model Number 12110
Hazard
The catheters may not retain their shape.
Sold states
Worldwide - US Nationwide distribution.
Affected count
41200 units
Manufactured in
7611 Northland Dr N, N/A, Brooklyn Park, MN, United States
Products
DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT 10FR, Model Number 12110
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2481-2025More Medtronic Perfusion Systems recalls
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- FDA-Device2026-05-27Medtronic DLP Retrograde Cannula recalled for potential sterile barrier breach
- FDA-Device2026-05-27Medtronic GUNDRY Retrograde Cannula recalled for sterile barrier breach risk
- FDA-Device2026-05-27Medtronic DLP Retrograde Cannula recalled for sterile barrier breach risk
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