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Displaying 21 - 40 of 214
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Cardiosave IABPs—Yet Again—the Subject of a Class I Recall: FDA
News Daily News

Cardiosave IABPs—Yet Again—the Subject of a Class I Recall: FDA

Caitlin E. Cox
Caitlin E. Cox
August 17, 2023
Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA
News Daily News

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

Michael O'Riordan
Michael O'Riordan
August 10, 2023
Abbott to Stop Making Trifecta Surgical Aortic Valves
News Daily News

Abbott to Stop Making Trifecta Surgical Aortic Valves

Michael O'Riordan
Michael O'Riordan
July 31, 2023
TCTMD’s Top 10 Most Popular Stories for July 2023
News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for July 2023

Shelley Wood
Shelley Wood
July 31, 2023
FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction
News Daily News

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

Caitlin E. Cox
Caitlin E. Cox
July 27, 2023
Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath
News Daily News

Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

Shelley Wood
Shelley Wood
July 26, 2023
Class I Recall for 350,000 Medtronic Defibrillators: FDA
News Daily News

Class I Recall for 350,000 Medtronic Defibrillators: FDA

Michael O'Riordan
Michael O'Riordan
July 19, 2023
TCTMD’s Top 10 Most Popular Stories for June 2023
News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for June 2023

Shelley Wood
Shelley Wood
July 03, 2023
Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks
News Daily News

Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks

Caitlin E. Cox
Caitlin E. Cox
June 05, 2023
Some Rays of Hope for ‘Sorry State’ of Transplant Rejection
News Features

Some Rays of Hope for ‘Sorry State’ of Transplant Rejection

Shelley Wood
Shelley Wood
May 08, 2023
The More Tweaks Made to PMA-Approved Devices, the More Likely a Recall
News Daily News

The More Tweaks Made to PMA-Approved Devices, the More Likely a Recall

Caitlin E. Cox
Caitlin E. Cox
April 13, 2023
Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs
News Daily News

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

Shelley Wood
Shelley Wood
March 31, 2023
Generic Dabigatran Lots Pulled for Nitrosamine Impurity
News Daily News

Generic Dabigatran Lots Pulled for Nitrosamine Impurity

Michael O'Riordan
Michael O'Riordan
March 28, 2023
Second Recall in Less Than 2 Months for Cardiosave IABPs
News Daily News

Second Recall in Less Than 2 Months for Cardiosave IABPs

L.A. McKeown
L.A. McKeown
March 17, 2023
SAFE-AAA Flags Ongoing EVAR Device Risk and Urges More Surveillance
News Daily News

SAFE-AAA Flags Ongoing EVAR Device Risk and Urges More Surveillance

L.A. McKeown
L.A. McKeown
March 16, 2023
FDA: GE Healthcare Recalls Nuclear Medicine Systems Due to Patient Injury Risk
News Daily News

FDA: GE Healthcare Recalls Nuclear Medicine Systems Due to Patient Injury Risk

L.A. McKeown
L.A. McKeown
February 16, 2023
New IABP Recall: Balloon Catheter Damage Might Cause Bleeding Into Pump
News Daily News

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

Shelley Wood
Shelley Wood
January 25, 2023
Medical Devices Cleared on Faulty Predicates More Likely to be Recalled
News Daily News

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

Michael O'Riordan
Michael O'Riordan
January 17, 2023
Paclitaxel Safety Concerns Wane as Hope Emerges for Newer PAD Devices
News Conference News

Paclitaxel Safety Concerns Wane as Hope Emerges for Newer PAD Devices

L.A. McKeown
L.A. McKeown
November 18, 2022
FDA: New Fix Available for Medtronic’s Troubled HeartWare VADs
News Daily News

FDA: New Fix Available for Medtronic’s Troubled HeartWare VADs

Michael O'Riordan
Michael O'Riordan
October 17, 2022

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