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Philips Ultrasound, Inc. recalls Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200), EPIQ 7C (Model # 795201), EPIQ 7W (Model # 7
Recalled November 15, 2023 · FDA recall Z-0283-2024 · Philips Ultrasound
Hazard
Their is the potential that diagnostic ultrasound systems operating with software version 10.0 may present a delayed image instead of a real time image. · FDA Class II
Units
83 systems
Sold at
US: AZ, CA, CT, FL, GA, ID, IL, KY, MD, MT, NE, NV, OH, TN, TX, UT, VA OUS: Canada
Description
Their is the potential that diagnostic ultrasound systems operating with software version 10.0 may present a delayed image instead of a real time image.
Product
Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200), EPIQ 7C (Model # 795201), EPIQ 7W (Model # 795202), EPIQ 5G (model # 795204), EPIQ 5W (model # 795206), EPIQ CVx (Model # 795231), EPIQ Elite (model # 795234)
Manufacturer(s)
Philips Ultrasound, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →