Home / Recalls / Medical Devices
Physio-Control, Inc. recalls The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and a
Recalled March 15, 2017 · FDA recall Z-1257-2017 · Physio-Control
Hazard
The firm has received complaints that the LIFEPAK 1000 Defibrillator is unexpectedly powering off during device usage. · FDA Class I
Units
total 133,330 units (50,046 units in the US)
Sold at
Worldwide Distribution - US (nationwide) and in the following countries: Bahrain, Belize, Cambodia, Chile, China, C¿te d'Ivoire, Ecuador, Germany, Honduras, Hong Kong, India, Indonesia, Jamaica, Myanmar, Netherlands, Niger, Philippines, Saudi Arabia, Senegal, Singapore, Sri Lanka, Thailand, Tunisia, Ukraine, and Zambia.
Description
The firm has received complaints that the LIFEPAK 1000 Defibrillator is unexpectedly powering off during device usage.
Product
The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR and the use of the LIFEPAK 1000 defibrillator.
Manufacturer(s)
Physio-Control, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →