FDAMarch 11, 2010device

The LIFEPAK 15 monitor/defibrillator is intended for use by trained medical personnel in outdoor and indoor emergency care settings within the environmental conditions specified. Product Part Numbers V-15-2-000XXX

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

The hazard

Customer complaint was received relating to a LifePak15 device that would power on then power down unexpectedly after a short period of use. When the LP15 powered down, power could be immediately restored by activation of the power button. The device was connected to a cellular modem from MultiTech systems for use with LIFE NET services. The corrective action was completed by Velocitor Solutions in December 2010.

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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