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Terminated

Syngo.plaza, Picture Archiving and Communication System

FDA Recall Z-2891-2016 · Posted 2016-09-27

Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeLLZ
Date Initiated2016-09-06
Date Terminated2017-05-08
Product Quantity47 systems

Reason for Recall

Software upgrade to eliminate several issues

Firm Action

Siemens notified customers via mail on 09/07/2016 informing them of the latest syngo.plaza software change that was available to address several issues.

Root Cause

Software design

Distribution Pattern

Distributed Nationwide

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K093612SYNGO.PLAZASiemens AG Medical Solutions · 2010-03-04

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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