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Philips Medical Systems, Inc. recalls Easy Diagnost Eleva Universal Fluoroscopic applications
Recalled December 11, 2013 · FDA recall Z-0431-2014 · Philips Medical Systems
Hazard
The delivered application software was an outdated version to the model of equipment. · FDA Class II
Units
19 devices
Sold at
Nationwide Distribution including MN, NH, DE, OR, MA, TX, OH, FL, CA, WA, and SC.
Description
The delivered application software was an outdated version to the model of equipment.
Product
Easy Diagnost Eleva Universal Fluoroscopic applications
Manufacturer(s)
Philips Medical Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →