FDAJanuary 12, 2017device

LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended for use on adult and pediatric patients. Automated external defibrillation mode is intended for use on patients eight years of age and older.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The firm has become aware of a potential device issue where the LIFEPAK 15 device may no longer be able to deliver defibrillation energy due to a potential failure of an internal component (Relay) installed on the Therapy Printed Circuit Board Assembly (PCBA).

What to do

FDA enforcement status: Terminated

Brands named

physio controlphysiophysio control

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended for use on adult and pediatric patients. Automated external defibrillation mode is intended for use on patients eight years of age and older. — Recall Details · AllClear