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Philips Healthcare Inc. recalls Philips IntelliVue Information Center/Client and Philips IntelliVue Information Center iX The intended use of the In
Recalled December 19, 2012 · FDA recall Z-0495-2013 · Philips Healthcare
Hazard
Internal audio cable may have diminished retention force due to damaged contacts, which could lead to intermittent or loss of audible alarms. · FDA Class II
Units
3165
Sold at
Worldwide Distribution - USA (nationwide) and Canada.
Description
Internal audio cable may have diminished retention force due to damaged contacts, which could lead to intermittent or loss of audible alarms.
Product
Philips IntelliVue Information Center/Client and Philips IntelliVue Information Center iX The intended use of the Information Center Software is to display physiologic waves, parameters, and trends, format data for strip chart recordings and printed reports, and provide the secondary annunciation of alarms from other networked medical devices at a centralized location. The Information Center Software provides for the retrospective review of alarms, physiologic waves and parameters from its database. An additional intended use of the Information Center Software is to provide primary annunciation of alarms and configuration and control access for networked telemetry monitors.
Manufacturer(s)
Philips Healthcare Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →