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AGFA Healthcare Corp. recalls AGFA DX-D 100 is a mobile digital radiography x-ray system
Recalled June 17, 2015 · FDA recall Z-1745-2015 · AGFA Healthcare
Hazard
When using the DX-D 100 unit, sporadic unintended movements caused by an electrostatic discharge of the unit to the ground may occur. · FDA Class II
Units
233 units
Sold at
US Distribution to the states of : AL, CA, DC, FL, GA, IL, IA, KY, LA, MD, MA, MI, MN, MS, MO, NE, NJ, NY, NC, OH, OK, OR, SC, TN, TX, VA, WV, WI and WY.
Description
When using the DX-D 100 unit, sporadic unintended movements caused by an electrostatic discharge of the unit to the ground may occur.
Product
AGFA DX-D 100 is a mobile digital radiography x-ray system
Manufacturer(s)
AGFA Healthcare Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →