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May 15, 2024

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HeartMate II and 3 LVADs Recalled Due to Potential for Outflow Graft Obstruction

April 22, 2024

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Label for Impella RP Flex Catheters Recalled to Address Anticoagulant Confusion: FDA

August 18, 2023

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Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA

August 10, 2023

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FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

July 27, 2023

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Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

March 31, 2023

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Second Recall in Less Than 2 Months for Cardiosave IABPs

March 17, 2023

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New IABP Recall: Balloon Catheter Damage Might Cause Bleeding Into Pump

January 25, 2023

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Medtronic Recalls Batteries in Some HeartWare VAD Systems

June 23, 2022

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Medtronic’s HeartWare HVAD Recalled for Pump Weld Defect

April 29, 2022

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FDA: Another Class I Recall for HeartWare VAD

April 16, 2021

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FDA: Class I Recall for HeartWare VAD Pump Implant Kit

March 01, 2021

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FDA: Class I Recall for Cardiosave Hybrid IABP Due to ‘Fluid Ingress’

June 07, 2018

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Class I Recall for Medtronic’s HeartWare HVAD System

June 04, 2018

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HeartMate 3 Problem With Outflow Graft Twisting Called Class I Recall by FDA

Todd Neale

May 23, 2018

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TCTMD’s Top 10 Most Popular Stories for June 2017

July 03, 2017

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HeartMate II Left Ventricular Assist System Under Recall Due to Controller Exchange Problems

Todd Neale

May 24, 2017

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FDA Classifies Latest HeartWare VAD Recalls as Class I

October 24, 2016

News Daily News

FDA Warns of Class I Recall for HeartWare VAD Batteries