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ZOLL Medical Corporation recalls Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Version 02.10.02.00 or
Recalled April 9, 2014 · FDA recall Z-1311-2014 · ZOLL Medical
Hazard
Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop and cannot be used · FDA Class II
Units
3,169 units
Sold at
Worldwide Distribution - USA (nationwide) and Internationally to Canada, AE, Afganistian, Australia, Belgium, Czech Republic , China, Chile, Croatia, Denmark, France, Great Britain, Hungary, Israel, Italy, Japan, Korea, Kuwait, Russia, Saudi Arabia, Singapore, South Africa,Thailand, and Turkey.
Description
Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop and cannot be used
Product
Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Version 02.10.02.00 or Higher, automated external defibrillator.
Manufacturer(s)
ZOLL Medical Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →