Medtronic Perfusion Systems recalls

22 recalls on record · latest: April 21, 2026

Official U.S. recall history for Medtronic Perfusion Systems, compiled from official government records.

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Medtronic Perfusion Systems recalls Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmonary bypass vascular ca…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonary bypass vascular cathe…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94965; Cardiopulmonary bypass vascular cathet…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary bypass vascular cathet…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular cathet…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular ca…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonary bypass vascular cathe…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary bypass vascular cathet…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular cathet…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1

January 13, 2026 · Medical device recalls Moderate risk During the manufacturing, Medtronic personnel identified an assembly issue wher…

Medtronic Perfusion Systems recalls Medtronic HR-ACT (High Range Activated Clotting Time Cartridges), REF 402-03

October 20, 2025 · Medical device recalls Moderate risk Medtronic personnel observed trace amounts of dry blood on the external carton…

Medtronic Perfusion Systems recalls MC3 VitalFlow Console, REF 58100; Blood pump of ecmo

October 3, 2025 · Medical device recalls Moderate risk As of August 6, 2025, Medtronic has received eleven reports of VitalFlow Consol…

Medtronic Perfusion Systems recalls Affinity NT Oxygenator, Oxygenator with Balance Biosurface and Uncoated Cardiotomy/Venous Reservoir, Product Number 541B

September 12, 2025 · Medical device recalls Moderate risk Medtronic identified an Affinity NT Oxygenator unit with decreased CO2 gas tran…

Medtronic Perfusion Systems recalls DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113 LV VENT 13FR, Model Number 12113

August 6, 2025 · Medical device recalls High risk The catheters may not retain their shape.

Medtronic Perfusion Systems recalls DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12115 LV VENT 15FR, Model Number 12115

August 6, 2025 · Medical device recalls High risk The catheters may not retain their shape.

Medtronic Perfusion Systems recalls DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT 10FR, Model Number 12110

August 6, 2025 · Medical device recalls High risk The catheters may not retain their shape.

Medtronic Perfusion Systems recalls Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA, model no 11012 B. CANNULA 11014 AR…

February 5, 2025 · Medical device recalls High risk Unexpected loose material in the male luer used in the aortic root cannula has…

Select Series Angled Tip Arterial Cannula recalled over labeling errors

December 12, 2024 · Medical device recalls Moderate risk Incorrect labeling for seven manufactured lots of certain models of Arterial Ca…

EOPA Arterial Cannula recalled over labeling errors

December 12, 2024 · Medical device recalls Moderate risk Incorrect labeling for seven manufactured lots of certain models of Arterial Ca…

DLP Pediatric One-Piece Arterial Cannulae recalled over labeling errors

December 12, 2024 · Medical device recalls Moderate risk Incorrect labeling for seven manufactured lots of certain models of Arterial Ca…

Medtronic Perfusion Systems recalls Medtronic DLP Aortic Root Cannula with Flow-Guard, REF 11012; for use in cardiopulmonary bypass surgery

October 3, 2024 · Medical device recalls Moderate risk There is the potential for a potential sterility breach for three lots of the D…

Medtronic Perfusion Systems recalls Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312

July 9, 2024 · Medical device recalls Moderate risk During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66…