Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0761-2017 — 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

U.S. FDA — Device Enforcement · United States · 2010-03-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0761-2017
Date of alert
2010-03-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Physio-Control, Inc.
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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