Medical device manufacturer Welch Allyn is recalling approximately 14,000 external defibrillators after 39 reported incidents, including two deaths. The recall involves 14,054 AED 10 and MRL JumpStart external defibrillators manufactured between October 3, 2002 and January 25, 2007. According to Welch Allyn there is the possibility that these prescription devices are susceptible to electromagnetic interference, may deliver low energy shock, or may shutdown unexpectedly. If these issues prevent defibrillation in a patient in cardiac arrest, the outcome would be fatal.For additional details, visit the Welch Allyn website.
Interference vs. Defibrillators
