Medical Product Manufacturer Announces Recall of AED Devices
Last week, the Cardiac Science Corporation notified the Food & Drug Administration (FDA) of the voluntary recall of approximately 12,200 automated external defibrillators (AEDs). Manufactured between October 19, 2009 and January 15, 2010, the devices began to fail under certain conditions, though these conditions were not listed. The company stated that the failure is being attributed to a manufacturing defect.
While the company claims that it has not received reports of the problem from external sources or customers- the problem was found through internal testing- a defect like this can lead to serious medical complications, including death. AEDs are used to treat victims thought to be experiencing cardiac arrest; the devices attach to the victim and then provide prompts to guide rescuers through rehabilitation steps. The devices also analyze heart rhythms and determine if defibrillation shock is necessary for resuscitation.
Continue reading "Medical Product Manufacturer Announces Recall of AED Devices" »


