Please provide your email address to receive an email when new articles are posted on . The FDA designated Defibtech’s recall of its automated continuous chest compression device as class I, the most ...
The recall is in response to a problem with the device’s motor that causes chest compressions to stop, which has resulted in one injury and one death, according to an Aug. 22 news release from the FDA ...
MINEOLA, Long Island (WABC) -- A new device to help save lives is coming to Nassau County. The Defibtech Lifeline Automated Chest Compression Device will go into every police department ambulance in ...
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