Syngo.plaza, picture archiving and communications system.
FDA Recall Z-1116-2017 · Posted None
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Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeLLZ
Date Initiated2017-01-11
Date Terminated2017-11-16
Product Quantity62 systems
Reason for Recall
Software update for improvements and to resolve several issues
Firm Action
Siemens mailed a Customer Letter to affected customers on 01/13/2017 to provide information about the latest software change that is now available to address several issues.
Root Cause
Under Investigation by firm
Distribution Pattern
Distributed throughout the United States.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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