Cangzhou Don’t let your AED become out of date from American Heart Association (AHA) guidelines. AEDs are designed to be updated. Also, all major AED manufacturers and their models have had software or hardware upgrades through FDA field corrective actions or FDA equipment recall notices. Extend the life of your AED as much as possible through our comprehensive database of AED recalls and updates available (most of which are free). To get a current list of AED recalls for 2021 and going forward to add to the below list please contact us by filling out the form or email us at info@think-safe.com with your question.
buy Lyrica online from mexico PS – Check to make sure your AED is still FDA Approved! In the past year, all major AED manufacturers have made announcements that they are discontinuing some of their AED lines.
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buy Lyrica uk Recall Date:Â 05/21/2010 Title:Â Defibtech LLC, DBP-2800 Battery Pack for ReviveR AED Units:Â DBP-2800 Battery Pack for the Defibtech ReviveR AED Fix:Â Contact Defibtech for correction
Recall Date:Â 02/03/2010 Title:Â Cardiac Science Notifies AED Customers of Voluntary Medical Device Recall Fix:Â If on the list, remove from service immediately. CS will replace the AED
Recall Date:Â 11/13/2009 Title:Â Voluntary Medical Device Correction: AED resistor and AED relay Fix:Â Install mandatory software update on all models Alert Documentation
Recall Date:Â 10/09/2009 Title:Â Factory-Testing Corrective Action Fix:Â If on the list, send unit to CS for testing
Recall Date:Â 07/31/2009 Title:Â Physio-Control Inc., LIFEPAK CR Plus Automated External Defibrillators (AEDs) Units:Â Physio-Control LIFEPAK CR PLUS AEDs with the serial numbers below are affected by this
Recall Date:Â 02/25/2009 Title:Â Welch Allyn AED 10 Recall Information Units:Â Welch Allyn AED10 or MRL JumpStart defibrillator* Part numbers 970300x, 970302x, 970308x, 970309x, 970310x, 970311x, where “x”
Recall Date:Â 02/12/2009 Title:Â ZOLL Medical Corporation, ZOLL AED Plus Defibrillator, Class 1 Recall Units:Â ZOLL AED Plus Defibrillator, Class 1 Recall Units Recalled: This product was manufactured
Recall Date: 10/30/2008 Title:Â 2008 CR Plus recall: Units:Â LIFEPAK CR Plus Issue:Â This recall is being conducted due to the device being configured with the incorrect software
Recall Date:Â 10/30/2008 Title:Â CR Plus 2008 recall: Units:Â LIFEPAK CR Plus Issue:Â The device may not power on although it indicates it is ready for use and would
Recall Date: 10/30/2008 Title: 2008 Lifepak Express recall: Units: LIFEPAK Express Issue: The device may not power on although it indicates it is ready for use and would not
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