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Skytron, Div. The KMW Group, Inc recalls Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical appli
Recalled January 20, 2016 · FDA recall Z-0655-2016 · Skytron, Div. The KMW Group
Hazard
The hardware that holds the VESA plate and the display interface / monitor to the bracket may fail causing the display interface to fall from the bracket. Over time and with use the threaded rod hardware material can weaken and detach from the bracket. A display interface falling from its mounting location may result in injury to the patient or provider. · FDA Class II
Units
286
Sold at
Worldwide Distribution - US including WI, TX, FL, NC, MD, OH, AZ, CA, UT, MT, OK, HI, CO, WY, MO, NJ, IL, NY, MA, IA, DE, PA, MI, IN, and WV and Internationally to Canada, and Japan.
Description
The hardware that holds the VESA plate and the display interface / monitor to the bracket may fail causing the display interface to fall from the bracket. Over time and with use the threaded rod hardware material can weaken and detach from the bracket. A display interface falling from its mounting location may result in injury to the patient or provider.
Product
Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical applications for viewing purposes and to provide an articulating point of movement on the ceiling mounted radial arm suspension system of the Ergon 2 equipment pendant / booms
Manufacturer(s)
Skytron, Div. The KMW Group, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →