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Cynosure, Inc. recalls Elite XPL (Pulsed Light) Handpiece for the Cynosure Elite MPX Laser System
Recalled November 12, 2014 · FDA recall Z-0169-2015 · Cynosure
Hazard
If the laser system is turned on and the user adjusts, installs or removes the XPL pulsed light handpiece, there is a potential risk of an electrical shock · FDA Class II
Units
322 units
Sold at
Worldwide Distribution - Nationwide Distribution and the countries of : Australia, Canada, France, Germany, Italy, Netherlands, Ukraine and UK.
Description
If the laser system is turned on and the user adjusts, installs or removes the XPL pulsed light handpiece, there is a potential risk of an electrical shock
Product
Elite XPL (Pulsed Light) Handpiece for the Cynosure Elite MPX Laser System
Manufacturer(s)
Cynosure, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →