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News Daily News

FDA Scolds Abiomed for Not Seeking a PMA for Its Web-Based User Portal

Caitlin E. Cox

October 17, 2023

News Daily News

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

Caitlin E. Cox

August 18, 2023

News Daily News

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

Caitlin E. Cox

August 17, 2023

News Daily News

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

Michael O'Riordan

August 10, 2023

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for July 2023

Shelley Wood

July 31, 2023

News Daily News

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

Caitlin E. Cox

July 27, 2023

News Daily News

Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

Shelley Wood

July 26, 2023

News Daily News

Class I Recall for 350,000 Medtronic Defibrillators: FDA

Michael O'Riordan

July 19, 2023

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for June 2023

Shelley Wood

July 03, 2023

News Daily News

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

Caitlin E. Cox

June 05, 2023

News Daily News

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

Caitlin E. Cox

April 13, 2023

News Daily News

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

Shelley Wood

March 31, 2023

News Daily News

Second Recall in Less Than 2 Months for Cardiosave IABPs

L.A. McKeown

March 17, 2023

News Daily News

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

L.A. McKeown

March 16, 2023

News Daily News

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

L.A. McKeown

February 16, 2023

News Conference News STS 2023

Earlier, More-Active Surgeon Involvement Needed in PE Care: AHA

Yael L. Maxwell

January 27, 2023

News Daily News

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

Shelley Wood

January 25, 2023

News Daily News

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

Michael O'Riordan

January 17, 2023

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FDA Scolds Abiomed for Not Seeking a PMA for Its Web-Based User Portal

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

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

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

TCTMD’s Top 10 Most Popular Stories for July 2023

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

Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

Class I Recall for 350,000 Medtronic Defibrillators: FDA

TCTMD’s Top 10 Most Popular Stories for June 2023

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

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

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

Second Recall in Less Than 2 Months for Cardiosave IABPs

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

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

Earlier, More-Active Surgeon Involvement Needed in PE Care: AHA

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

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

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