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  • News (47)
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Displaying 1 - 20 of 47
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Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA
News Daily News

Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA

Yael L. Maxwell
Yael L. Maxwell
April 03, 2024
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
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
Recall for Mislabeled Cartons of Amiodarone, Tranexamic Acid Injections: FDA
News Daily News

Recall for Mislabeled Cartons of Amiodarone, Tranexamic Acid Injections: FDA

Shelley Wood
Shelley Wood
September 01, 2020
FDA: Class I Recall for Medtronic’s Pipeline Flex and Pipeline Flex With Shield Technology
News Daily News

FDA: Class I Recall for Medtronic’s Pipeline Flex and Pipeline Flex With Shield Technology

Caitlin E. Cox
Caitlin E. Cox
March 31, 2020
FDA: Abbott Recalls NC Trek RX and NC Traveler Coronary Catheters
News Daily News

FDA: Abbott Recalls NC Trek RX and NC Traveler Coronary Catheters

Shelley Wood
Shelley Wood
February 24, 2020
FDA: Obesity Drug Lorcaserin Exits US Market Over Cancer Concerns
News Daily News

FDA: Obesity Drug Lorcaserin Exits US Market Over Cancer Concerns

Shelley Wood
Shelley Wood
February 14, 2020
News Daily News

CV Safety Trial for Lorcaserin Picks Up Cancer Signal: FDA

Shelley Wood
Shelley Wood
January 14, 2020
FDA Is Surveilling Heparin but Believes Defective Quality Unlikely
News Daily News

FDA Is Surveilling Heparin but Believes Defective Quality Unlikely

Yael L. Maxwell
Yael L. Maxwell
December 06, 2019
Subtherapeutic Heparin: As Stories Multiply, Concerns Mount
News Features

Subtherapeutic Heparin: As Stories Multiply, Concerns Mount

Yael L. Maxwell
Yael L. Maxwell
November 27, 2019
FDA: Class I Recall for CentriMag Circulatory Support System Motor
News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

Caitlin E. Cox
Caitlin E. Cox
November 07, 2019
FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device
News Daily News

FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device

Shelley Wood
Shelley Wood
July 02, 2019
FDA Warns Healthcare Providers of Potential Rise in Death Rate With Impella RP
News Daily News

FDA Warns Healthcare Providers of Potential Rise in Death Rate With Impella RP

Caitlin E. Cox
Caitlin E. Cox
February 04, 2019
FDA Alerts Doctors to Potential Late Risks With Paclitaxel-Coated Balloons and Stents in PAD
News Daily News

FDA Alerts Doctors to Potential Late Risks With Paclitaxel-Coated Balloons and Stents in PAD

Michael O'Riordan
Michael O'Riordan
January 17, 2019
FDA: All AFX Endovascular AAA Systems Now Under Class I Recall
News Daily News

FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

L.A. McKeown
L.A. McKeown
October 16, 2018
FDA Warns of Deaths, Stroke With Latest-Generation Total Artificial Heart
News Daily News

FDA Warns of Deaths, Stroke Due to Power System Problems With Total Artificial Heart System

Lucy Hicks
Lucy Hicks
August 17, 2018
News Daily News

FDA Posts Outdated Alert for Sapien 3 Transapical Delivery System

Shelley Wood
Shelley Wood
January 11, 2018
FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair
News Daily News

FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair

L.A. McKeown
L.A. McKeown
October 02, 2017
News Industry News

AstraZeneca Initiates Voluntary Nationwide Recall of One Lot of BRILINTA 90mg Professional Sample Bottles Due to Report of Another Medicine in One Bottle from That Lot

May 26, 2017
FDA Warns of Risk of Major Adverse Cardiac Events With Absorb BVS
News Conference News ACC 2017

FDA Warns of Risk of Major Adverse Cardiac Events With Absorb BVS

Michael O'Riordan
Michael O'Riordan
March 18, 2017

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