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Class I Recall for 350,000 Medtronic Defibrillators: FDA

News Daily News

Class I Recall for 350,000 Medtronic Defibrillators: FDA

Michael O'Riordan

July 19, 2023

FDA Provides Update on Poorer Survival With Impella RP in Postmarket Setting

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FDA Provides Update on Poorer Survival With Impella RP in Postmarket Setting

May 21, 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

February 04, 2019

News Daily News

Recall Underway for AED Electrodes With Compatibility Problems

October 17, 2016

News Daily News

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

Michael O'Riordan

June 08, 2016

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