Company:Hitachi Medical Systems America, Inc.Date of Enforcement Report:6/7/2006 Class:lI PRODUCT Magnetic Resonance Imaging Device, Recall # Z-0910-06 REASON The device has a software anomaly which causes the operating system to lock up and data to become corrupted during service procedures. CODE L001-L223 C002-C765 Hoo2-H733 RECALLING FIRM/MANUFACTURER Recalling Firm: Hitachi Medical Systems America, Inc., Twinsburg, OH,...Read More
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