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    Pioneer Catheter (Crosspoint TransAccess Catheter); Model TA-XP-001; Product is manufactured and distributed by Medtronic Vascular, Santa Rosa, CA 95403

    FDA Recall
    Terminated ·Medtronic Vascular·Product code ITX·November 1, 2006

    Medtronic EnVeo R Delivery Catheter System (DCS), Models: ENVEOR-L, ENVEOR-L-C, and ENVEOR-US. Designed to replace the native or surgical bioprosthetic aortic heart valve without open heart surgery and without concomitant surgical removal of the failed valve.

    FDA Recall
    Terminated ·Medtronic Cardiovascular Surgery-the Heart Valve Division·Product code NPT·August 3, 2016

    Medtronic Venous Cannula with bent tip wire, for vascular cardiopulmonary bypass. Catalog Number: CB67532

    FDA Recall
    Terminated ·Medtronic Perfusion Systems·Product code DWF·May 9, 2008

    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code DWF·April 21, 2026

    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary bypass vascular catheter

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code DWF·April 21, 2026

    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94965; Cardiopulmonary bypass vascular catheter

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code DWF·April 21, 2026

    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular catheter

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code DWF·April 21, 2026

    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary bypass vascular catheter

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code DWF·April 21, 2026

    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonary bypass vascular catheter

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code DWF·April 21, 2026

    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonary bypass vascular catheter

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code DWF·April 21, 2026

    Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code DWF·April 21, 2026

    Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmonary bypass vascular catheter

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code DWF·April 21, 2026

    Medtronic Malleable Single Stage Venous Cannula with Carmeda BioActive Surface, for Vascular Cardiopulmonary Bypass. Catalog Number: CB68122

    FDA Recall
    Terminated ·Medtronic Perfusion Systems·Product code DWF·May 9, 2008

    Medtronic IN.PACT AV, Paclitaxel-coated PTA Balloon Catheter, REF: IAV06008008P, Sterile EO, Rx Only

    FDA Recall
    Open, Classified ·Medtronic Vascular, Inc.·Product code PRC·March 23, 2022

    Medtronic Catheter, Cannula and Tubing, for Vascular Cardiopulmonary Bypass. This product is only available OUS. Catalog number: M470450E

    FDA Recall
    Terminated ·Medtronic Perfusion Systems·Product code DWF·May 9, 2008

    Medtronic 6F Zuma Guide Catheter with AL 1.5 Curve with side holes Catalog Number: Z26AL15SH The Medtronic Guiding Catheter is designed to provide a pathway through which therapeutic devices are introduced. The guiding catheter is intended to be used in the coronary or peripheral vascular system.

    FDA Recall
    Terminated ·Medtronic Vascular·Product code DQY·June 8, 2011

    Angiographic Guidewire Component: Model Number: 107042, 107044, 107447, 110003, 110004, The angiographic guidewire components associated with this recall are manufactured with a requirement that further downstream processing (sterilization) is required. Indications for use for these components are not defined as they are not intended for final use.

    FDA Recall
    Terminated ·Medtronic Vascular·Product code NKQ·May 4, 2021

    SHERPA NX ACTIVE GUIDING CATHETER, 6F, JL4.0, 110CM, 070", REF SA6JL40A. for cardiovascular use

    FDA Recall
    Terminated ·Medtronic Vascular·Product code DQY·March 15, 2019

    SHERPA NX ACTIVE GUIDING CATHETER, 6F AL2.0, .070", REF SA6AL20. for cardiovascular use

    FDA Recall
    Terminated ·Medtronic Vascular·Product code DQY·March 15, 2019

    SHERPA NX ACTIVE GUIDING CATHETER, 6F CHAMP3.0, .070", REF SA6CHAMP30. for cardiovascular use

    FDA Recall
    Terminated ·Medtronic Vascular·Product code DQY·March 15, 2019