Cardiac Science Automated External Defibrillators (Powerheart, Cardiovive, CardioLife models): Recall

by FDA on February 12, 2010

in MedWatch

Device may not be able to deliver therapy during a cardiac resuscitation attempt.

This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program. The link below will take you to the original notice.

View Full Details Of The Original MedWatch Notice Here.

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