FDAFebruary 1, 2019device

LIFEPAK 15 Monitor/Defibrillator service kits Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient management protocols. The LP15 monitor/defibrillator is intend...

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

The hazard

Certain LIFEPAK 15 Monitors/ Defibrillators were reported to experience a lockup condition after a shock was delivered. This condition is defined as a blank monitor display with LED lights on, indicating power on the device, but no response in keypad and device functions.

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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