Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0524-2018 — Syngo.plaza systems with SW VB20A, Model Number - 10863171, 10863172, 10863173 Product Usage: Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physicia

U.S. FDA — Device Enforcement · United States · 2017-08-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0524-2018
Date of alert
2017-08-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Medical Solutions USA, Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10863171
Reported risk: When a prior study is being replaced in the workflow step, in certain scenarios (based on the Display Protocol configuration) the prior study will only be replaced in the active Workflow Step and not show in all other workflow steps. The other workflow steps will continue to show the initially loaded study.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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