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AED Heart Device Deaths
Contact Anapol Schwartz to Investigate Your Claim Against Powerheart, Cardiovive, CardioLife AEDs by Cardiac Science Corporation
Was your loved one’s death caused by a failed Powerheart, Cardiovive, CardioLife AED? According to the FDA Warning to Emergency medical professionals, Powerheart, Cardiovive, CardioLife models have been recalled by Cardiac Science Corporation due to the automated external defibrillator failing to deliver appropriate treatment during a cardiac resuscitation attempt. This failure can lead to death. The products are alleged to be susceptible to failure.
Devices affected by this recall can be found here. The AEDs were made or serviced between 10/19/2009 and 1/15/2010. These include Powerheart models 9300A, 9300E, 9300P, 9390A, 9390E, CardioVive model 92532 and CardioLife models 9200G and 9231.
Each affected AED should immediately be removed from service since it may not deliver the expected therapy. Pleases see: The FDA Press release on this product for more information.
Anapol Schwartz Heart Device Lawyers are ready to analyze your claims. Call us toll free at 866-735-2792 or please fill out the case form on the side of this page if you believe that you or a loved one has been harmed by this device.
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