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Medtronic Perfusion Systems recalls DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113 LV VENT 13FR, Model Number 12113
Recalled September 10, 2025 · FDA recall Z-2480-2025 · Medtronic Perfusion Systems
Hazard
The catheters may not retain their shape. · FDA Class I
Units
34549 units
Sold at
Worldwide - US Nationwide distribution.
Description
The catheters may not retain their shape.
Product
DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113 LV VENT 13FR, Model Number 12113
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →