April 23, 2010 (Rockville, Maryland) — The Food and Drug Administration has issued a class 1 recall of the LIFEPAK 15 Monitor/Defibrillator (Physio-Control, Redmond, WA) [1]. The recall affects ...
The company is notifying certain LIFEPAK 15 customers of an issue that may cause the device to lock up after a defibrillation shock is delivered. The lock-up condition is defined as a blank monitor ...
KALAMAZOO, Mich. — Two medical teams in Michigan are working together to launch the "nex gen" defibrillator. Life EMS, a West Michigan-owner provider, is anticipated to be the first emergency service ...
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