Z-1311-2014 Class II Terminated
Recall Details
- Product Type
- Devices
- Report Date
- April 9, 2014
- Initiation Date
- March 5, 2014
- Termination Date
- January 29, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3,169 units
Product Description
Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Version 02.10.02.00 or Higher, automated external defibrillator.
Reason for Recall
Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop and cannot be used
Distribution Pattern
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.
Code Information
System Software Version 02.10.02.00 or Higher