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Philips Electronics North America Corporation recalls Philips DigitalDiagnost 3.1.x X-Ray System
Recalled June 21, 2017 · FDA recall Z-2154-2017 · Philips Electronics North America
Hazard
During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have identified a potential issue that may affect the performance of the equipment under certain conditions. · FDA Class II
Units
US - 132
Sold at
USA(nationwide) Distribution to the states of : AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, IL, IN, KY, LA, MA, ME, MI, MN, MO, NC, ND, NE, NH, NM, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA and WI
Description
During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have identified a potential issue that may affect the performance of the equipment under certain conditions.
Product
Philips DigitalDiagnost 3.1.x X-Ray System
Manufacturer(s)
Philips Electronics North America Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →