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Dragonfly OpStar OCT Catheter Recalled for Loose Marker Band

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Dragonfly OpStar OCT Catheter Recalled for Loose Marker Band

May 26, 2022

Medtronic’s HeartWare HVAD Recalled for Pump Weld Defect

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Medtronic’s HeartWare HVAD Recalled for Pump Weld Defect

April 29, 2022

Medtronic Recalls Harmony Delivery Catheters Due to Breakage Risk

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Medtronic Recalls Harmony Delivery Catheters Due to Breakage Risk

April 26, 2022

Medtronic Recalls TurboHawk Plus Atherectomy System

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Medtronic Recalls TurboHawk Plus Atherectomy System

March 09, 2022

HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

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HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

January 21, 2022

FDA Safety Communication Updates Stance on Endologix AAA Grafts

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FDA Safety Communication Updates Stance on Endologix AAA Grafts

January 13, 2022

Wirion Embolic Protection System Recalled Over Filter Breakage

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Wirion Embolic Protection System Recalled Over Filter Breakage

January 10, 2022

Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

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Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

December 22, 2021

Class I Recall of Batteries for Cardiosave Hybrid/Rescue IABPs: FDA

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Class I Recall of Batteries for Cardiosave Hybrid/Rescue IABPs: FDA

October 29, 2021

Class I Recall for Cordis’ Super Torque Catheters with Radiopaque Markers

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Class I Recall for Cordis’ Super Torque Catheters with Radiopaque Markers

Michael O'Riordan

September 23, 2021

News Industry News

Cardiologs Unveils New Solution to Enable Use of Smartwatches for Remote Patient Monitoring

July 21, 2021

Medtronic Vascular Recalls Angiographic Guidewire Components

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Medtronic Vascular Recalls Angiographic Guidewire Components

July 02, 2021

FDA: Class I Recall of Precise PRO Rx Carotid Stent System

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FDA: Class I Recall of Precise PRO Rx Carotid Stent System

April 23, 2021

FDA: Another Class I Recall for HeartWare VAD

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FDA: Another Class I Recall for HeartWare VAD

April 16, 2021

FDA: Class I Recall for Seven Models of Medtronic ICDs and CRT-Ds

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FDA: Class I Recall for Seven Models of Medtronic ICDs and CRT-Ds

Yael L. Maxwell

April 12, 2021

FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

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FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

December 16, 2020

CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

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CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

July 01, 2020

Medtronic Recalls Parts of Its HeartWare VAD System

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Medtronic Recalls Parts of Its HeartWare VAD System

May 29, 2020

FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

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FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

December 17, 2019

FDA: New Concerns Surface With Endologix Grafts for AAA

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FDA: New Concerns Surface With Endologix Grafts for AAA

October 28, 2019

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