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Philips Healthcare recalls Philips Healthcare DuraDiagnost stationary X-ray system
Recalled June 15, 2016 · FDA recall Z-1696-2016 · Philips Healthcare
Hazard
The detector may signal that it is ready for acquisition when it actually is not, resulting in failure to properly acquire the X-ray image. · FDA Class II
Units
5
Sold at
USA (nationwide) Distribution to the states of : ( DuraDiagnost) to the states of : OH, CA, WA and NE. (DigitalDiagnost) to the states of : AK, AZ, AL, CA, CT, CO, DE, FL, GA, HI, ID, KY, LA, MA, MN, MD, MS, ME, MO, NE, NY, ND, OH and PA.
Description
The detector may signal that it is ready for acquisition when it actually is not, resulting in failure to properly acquire the X-ray image.
Product
Philips Healthcare DuraDiagnost stationary X-ray system
Manufacturer(s)
Philips Healthcare
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →