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All product recalls associated with Hitachi Medical Systems America Inc.
Total Recalls
1000
Past Year
88
Class I (Serious)
98
Most Recent
Nov 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The device has a software anomaly which affects the system's ability to create Multiplanar Reconstructions (MPR). Some images from the resulting series do not display correctly, or display at all, when MPR was run on them.
The device has a software anomaly which causes blank images to be created during Multiplanar Reconstruction processing or results in an inherent filming error in which a reference scale is improperly sized.
The device has a software anomaly which causes the operating system to 'lock up' and data to become corrupted during service procedures.