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News Daily News

Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

Todd Neale

December 22, 2021

News Daily News

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

Caitlin E. Cox

October 29, 2021

News Daily News

FDA Investigating Possible Sex Differences in LAAO Outcomes

Todd Neale

September 27, 2021

News Daily News

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

Michael O'Riordan

September 23, 2021

News Daily News

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

L.A. McKeown

August 20, 2021

News Daily News

Medtronic Vascular Recalls Angiographic Guidewire Components

Todd Neale

July 02, 2021

News Daily News

Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

Michael O'Riordan

June 17, 2021

News Daily News

FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

L.A. McKeown

June 03, 2021

News Daily News

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

Caitlin E. Cox

April 23, 2021

News Daily News

FDA: Another Class I Recall for HeartWare VAD

Shelley Wood

April 16, 2021

News Daily News

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

Yael L. Maxwell

April 12, 2021

News Daily News

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Shelley Wood

March 01, 2021

News Daily News

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

Shelley Wood

February 17, 2021

News Daily News

FDA Issues Class I Recall for Emblem S-ICD Over Electrode Fractures

Michael O'Riordan

February 12, 2021

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Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

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

FDA Investigating Possible Sex Differences in LAAO Outcomes

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

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

Medtronic Vascular Recalls Angiographic Guidewire Components

Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

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

FDA: Another Class I Recall for HeartWare VAD

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

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

FDA Issues Class I Recall for Emblem S-ICD Over Electrode Fractures

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