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Displaying 21 - 40 of 41
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FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers
News Daily News

FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

Michael O'Riordan
Michael O'Riordan
May 07, 2019
FDA Warns of Cybersecurity Vulnerabilities With Some Medtronic Implanted Devices
News Daily News

FDA Warns of Cybersecurity Vulnerabilities With Some Medtronic Implanted Devices

Michael O'Riordan
Michael O'Riordan
March 22, 2019
Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue
News Daily News

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

Todd Neale
Todd Neale
February 27, 2019
Class I Recall for Certain Medtronic Pacemakers Due to Possible Circuit Error
News Daily News

Class I Recall for Certain Medtronic Pacemakers Due to Possible Circuit Error

Todd Neale
Todd Neale
February 15, 2019
More INR Test Strips Recalled Due to Inaccurately High Results
News Daily News

More INR Test Strips Recalled Due to Inaccurately High Results

Todd Neale
Todd Neale
December 21, 2018
INR Test Strips Recalled Due to Inaccurate Measurements
News Daily News

INR Test Strips Recalled Due to Inaccurate Measurements

Todd Neale
Todd Neale
November 02, 2018
FDA: Battery, Cybersecurity Issues With ICDs and CRT-Ds Now Have Firmware Fix
News Daily News

FDA: Battery, Cybersecurity Issues With ICDs and CRT-Ds Now Have Firmware Fix

Todd Neale
Todd Neale
April 17, 2018
Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs
News Daily News

Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs

Todd Neale
Todd Neale
February 27, 2018
FDA Warns Certain Zoll LifeVests Might Fail to Deliver Shocks
News Daily News

FDA Warns Certain Zoll LifeVests Might Fail to Deliver Shocks

Michael O'Riordan
Michael O'Riordan
January 17, 2018
News Daily News

Apixaban Recalled Following Complaints of Dose-Packaging Mismatch

Shelley Wood
Shelley Wood
June 13, 2017
News Daily News

FDA: Class I Recall for Over 47,000 HeartStart MRx Monitor/Defibrillator Units

L.A. McKeown
L.A. McKeown
March 24, 2017
News Daily News

FDA Warns of Cybersecurity Holes in Certain Cardiac Devices and Monitoring System

Yael L. Maxwell
Yael L. Maxwell
January 09, 2017
News Daily News

Recall Underway for AED Electrodes With Compatibility Problems

Todd Neale
Todd Neale
October 17, 2016
News Daily News

St. Jude Medical Warns of Rapid, Unexpected, and Potentially Lethal Battery Depletions With ICDs, CRT-Ds

Shelley Wood
Shelley Wood
October 11, 2016
News Daily News

FDA Declines to Approve Portola’s Reversal Agent for Factor Xa Inhibitors

Michael O'Riordan
Michael O'Riordan
August 18, 2016
News Daily News

FDA:凝血监测系统四面楚歌、境况堪忧

Todd Neale
Todd Neale
July 13, 2016
News Daily News

FDA: No More Chances for Embattled Coagulation Monitoring System

Todd Neale
Todd Neale
July 13, 2016
News Daily News

FDA: No Más Oportunidades para el Acosado Sistema para Monitorizar la Coagulación

Todd Neale
Todd Neale
July 13, 2016
News Daily News

止泻药洛哌丁胺的滥用与严重心脏事件包括死亡相关

Michael O'Riordan
Michael O'Riordan
June 08, 2016
News Daily News

Serious Cardiac Events, Including Death, Linked to Abuse of Antidiarrheal Medication Loperamide

Michael O'Riordan
Michael O'Riordan
June 08, 2016

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