43 results
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32ms
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Sources: EU EUDAMED, US FDA
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Status: Open, Classified
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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 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 IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model Numbers:ADM04004013P ADM04008013P ADM04008013P ADM04008013P ADM04012013P ADM04015013P ADM04015013P ADM04025013P ADM05004013P ADM05004013P ADM05006013P ADM05006013P ADM05008013P ADM05008013P ADM05020013P ADM06004013P ADM06004013P ADM06006013P ADM06006013P ADM06008013P ADM06012013P ADM06015013P ADM06015013P ADM06015013P ADM06015013P ADM07004013P ADM07006013P ADM07006013P ADM07008013P SBI04004013P SBI04008008P SBI04012013P SBI04015013P SBI05004008P SBI05006013P SBI05012008P SBI05012008P SBI05012013P SBI05015013P SBI06004008P SBI06004008P SBI06004013P SBI06004013P SBI06006008P SBI06006008P SBI06008008P SBI06008008P SBI06012013P SBI06012013S SBI06015013P SBI07004013P SBI08004013P SBI08008008S SBI10004008P
FDA Recall
Open, Classified
·Medtronic Vascular, Inc.·Product code ONU·March 23, 2022
Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T12BTNL
FDA Recall
Open, Classified
·Product code GCJ·February 28, 2024
Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BT
FDA Recall
Open, Classified
·Product code GCJ·February 28, 2024
Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BTSNL
FDA Recall
Open, Classified
·Product code GCJ·February 28, 2024
Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T12BT
FDA Recall
Open, Classified
·Product code GCJ·February 28, 2024
Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BTNL
FDA Recall
Open, Classified
·Product code GCJ·February 28, 2024
Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BTS
FDA Recall
Open, Classified
·Product code GCJ·February 28, 2024
Covidien Auto Suture" Structural Balloon Trocar, Product Number OMS-T10SB
FDA Recall
Open, Classified
·Product code GCJ·February 28, 2024
Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT ENTF2525C70EE ENDURANT TUBE
FDA Recall
Open, Classified
·Medtronic Vascular, Inc.·Product code MIH·October 15, 2021
Endurant II/Endurant IIs Stent Graft System: Medtronic Endurant II Stent Graft System REF ETUF3214C102EE, ETCF3636C49EE, ETBF3216C166EE, and ETUF3614C102E. Used to treat infrarenal abdominal aortic or aortoiliac aneurysms using an endovascular approach.
FDA Recall
Open, Classified
·Medtronic Vascular, Inc.·Product code MIH·June 7, 2021