Manufacturers
Quick Find
 
Use keywords to find the product you are looking for.
Advanced Search
What's New?

AED FDA/ Corrective Actions

Display: 

Info about AED recalls, corrective actions and notices

Displaying 1 to 10 (of 10 articles) Result Pages:  1 
Below is a list of articles with the most recent ones listed first.
Cardiac Science AED Recall January 2012 by Cardiac Science Corp. Topic: AED FDA / Corrective Actions
Cardiac Science AED Recall January 2012
Published: Tuesday 24 January, 2012
Zoll Gets FDA Warning Letter on Defibrillator Battery Life 4-22- Topic: AED FDA / Corrective Actions
Zoll Gets FDA Warning Letter over Battery Life
Published: Tuesday 30 August, 2011
Cardiac Science Customer Notification August 2011 Topic: AED FDA / Corrective Actions
New Cardiac Science Customer Notification Letter - August 2011
Published: Friday 26 August, 2011
Cardiac Science - Expanded Recall April 27, 2010 by Cardiac Science Corp. Topic: AED FDA / Corrective Actions
FDA Article on Expanded Scope of Cardiac Science Recals affecting approximately 280,000 AEDs. Defective Cardiac Science Corporation Powerheart, CardioVive, Nihon Kohden, and GE Responder External Defibrillators: Updated April 27, 2010
Published: Saturday 26 June, 2010
Zoll AED Plus Guidelines 2005 Upgrade by Zoll Medical Corp. Topic: AED FDA / Corrective Actions
Zoll AED Plus Guidelines 2005 Upgrade Information
Published: Monday 21 June, 2010
Defibtech Recall of DBP-2800 Battery Packs - June 3, 2010 Topic: AED FDA / Corrective Actions
Defibtech Announces a Voluntary Recall of DBP-2800 Battery Packs used in the Lifeline AEDŽ and ReviveR AED
Published: Monday 14 June, 2010
Philips Voluntary Medical Devise Recall by Philips Healthcare Topic: AED FDA / Corrective Actions
Philips Voluntary Medical Devise Recall - Limited OnSite and FRx AEDs made in March 2010
Published: Wednesday 02 June, 2010
Medtronic - Physio Control Corrective Action LP 20/20e - July 2, Topic: AED FDA / Corrective Actions
This article covers the Field Corrective Action to LIFEPAK 20/20e Defibrillator/Monitors - July 02, 2010. The affected devices were manufactured from July 31, 2002 to Sept. 19, 2007. The recall affects approximately 43,000 LIFEPAK 20 and LIFEPAK 20e defibrillator/monitors shipped globally to hos...
Published: Wednesday 21 April, 2010
Zoll AED Corrective Action 3/31/2009 by Zoll Medical Corp. Topic: AED FDA / Corrective Actions
This provides current information about the Zoll AED Plus Corrective Action
Published: Wednesday 21 April, 2010
Cardiac Science Manadatory Software Update by Cardiac Science Corp. Topic: AED FDA / Corrective Actions
Cardiac Science announced a mandatory software update for Field Correction: AED resistor and AED relay. Affects certain AEDs manufactured between August 2003 and August 2009.
Published: Wednesday 21 April, 2010
Displaying 1 to 10 (of 10 articles) Result Pages:  1