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PHILIPS MEDICAL SYSTEMS recalls CombiDiagnost R90 1.0 (709030)
Recalled February 21, 2024 · FDA recall Z-1087-2024 · PHILIPS MEDICAL SYSTEMS
Hazard
While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image content, image format and image size. · FDA Class II
Units
86 units
Sold at
US Nationwide distribution in the states of CA, FL, GA, IL, IN, KS, MD, ME, MI, MN, NC, NJ, NY, TX, VA, WA.
Description
While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image content, image format and image size.
Product
CombiDiagnost R90 1.0 (709030)
Manufacturer(s)
PHILIPS MEDICAL SYSTEMS
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →