Reported Apr 5, 2017 · Terminated

Syngo.via, Picture archiving and communication system Syngo via is a software solution intended to be used for viewing,…

Siemens Medical Solutions USA, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Siemens Medical Solutions USA, Inc · 40 Liberty Blvd · Malvern, PA · 19355-1418

Is this the product you have?

  • Syngo.via, Picture archiving and communication system Syngo via is a software solution intended to be used for viewing, manipulation, communication, and storage of medical images. It can be used as a standalone device or together with a variety of cleared and unmodified syngo based software options. Syngo.via supports interpretation and evaluation of examinations within healthcare institutions, for example, in Radiology, Nuclear Medicine and Cardiology environments. The system is not intended for the displaying of digital mammography images for diagnosis in the U.S. The system is a software only medical device. It defines minimum requirements to the hardware it runs on. The hardware itself is not seen as a medical device and not in the scope of this 510(k) submission. It supports the physician in diagnosis and treatment planning. Syngo.via also supports storage of Structured DICOM Reports. In a comprehensive imaging suite syngo.via integrates Radiology Information Systems (RIS) to enable customer specific workflows. Syngo.via allows to use a variety of advanced applications (clinical applications) designed for syngo.via just as the predicate device syngo.x,(K092519,cleared on August 27, 2009). These applications are medical devices on their own rights and filed separately. They are not part of this 510(k) submission and not part of the syngo.via medical device. Syngo.via has a universal component called generic reader application which is part of this medical device and it allows no newly introduced imaging and post processing algorithms compared to the above mentioned predicate devices. Syngo.via is based on Windows. Due to special customer requirements and the clinical focus syngo.via can be configured in the same way as the predicate device with different combinations of syngo- or Windows -based software options and clinical applications which are intended to assist the physician in diagnosis and/or treatment planning. This includes commercially available post-processing software packages. Syngo.via Data Management ...ensures all authorized personnel fast and continuous access to radiological data. It's main functionality ranges from availability of images with regard to data security, open interfaces, storage media and central system administration, to provide a flexible storage hierarchy.
Lot codes and dates
  • Device Model Numbers
    • 10863171
    • 10863172
    • 10863173
  • Serial Numbers

    104 of 104 codes

    • 401018
    • 221363
    • 221402
    • 310364
    • 222027
    • 221225
    • 130653
    • 310395
    • 310397
    • 221110
    • 130765
    • 310310
    • 450002
    • 130848
    • 130849
    • 130692
    • 310536
    • 131037
    • 221199
    • 131200
    • 130773
    • 401005
    • 130874
    • 130706
    • 401004
    • 310363
    • 400047
    • 131011
    • 130784
    • 401062
    • 310361
    • 221192
    • 221373
    • 401070
    • 222060
    • 310544
    • 310365
    • 310388
    • 310348
    • 221280
    • 401024
    • 130772
    • 310486
    • 130628
    • 130777
    • 130998
    • 131160
    • 222025
    • 221403
    • 221388
    • 221344
    • 131127
    • 222023
    • 130716
    • 221345
    • 310472
    • 130808
    • 221198
    • 130734
    • 310396
Amount recalled
104

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Software changes now available to address several issues

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 12, 2017 · Data as of Sep 19, 6:04 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.