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Hitachi Healthcare Americas Corp Informatics Division recalls VidiStar(TM) PACS & DICOM Viewer Software system
Recalled September 12, 2018 · FDA recall Z-2992-2018 · Hitachi Healthcare Americas Corp Informatics Division
Hazard
The secure filesystem client software used in the interface between the Vidistar PACS and an EHR system may cause intermixed images from multiple patients showing in a single study. · FDA Class II
Units
12 units
Sold at
SC, CO, IL, AZ, MT, OH, IN, TX, GA, MA
Description
The secure filesystem client software used in the interface between the Vidistar PACS and an EHR system may cause intermixed images from multiple patients showing in a single study.
Product
VidiStar(TM) PACS & DICOM Viewer Software system
Manufacturer(s)
Hitachi Healthcare Americas Corp Informatics Division
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →