Home / Recalls / Fujifilm Medical Systems U.S.A., Inc. / Z-2441-2019

Z-2441-2019 Class II Terminated

Recalled by Fujifilm Medical Systems U.S.A., Inc. — Lexington, MA

Recall Details

Product Type
Devices
Report Date
September 11, 2019
Initiation Date
July 19, 2019
Termination Date
August 28, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
174 units

Product Description

Fujifilm FDR Go Plus mobile X-ray system

Reason for Recall

The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD)

Distribution Pattern

Nationwide

Code Information

All serial numbers

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  • Z-2471-2020 Class II — Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as interface t (May 22, 2020)
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  • Z-0659-2018 Class II — Aspire HD (for FDR-1000AWS) The Fujifilm Digital Mammography System, Aspire H (August 4, 2017)