RecallRadar

FDA Device recall Z-2245-2016

Syngo.via, picture archiving and communications system software controlled

On 2016-07-27 the FDA classified a Class II recall of Syngo.via, picture archiving and communications system software controlled by Siemens Medical Solutions Usa, citing incorrect values for the volume calculation. Software update VB30B via Update Instructions SY018/16/P to resolve software errors.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2245-2016
ClassificationClass II
Statusterminated
Initiated2016-06-23
Published2016-07-27
Last updated2026-09-13 11:54 UTC
CompanySiemens Medical Solutions Usa
DistributionUS

Product

Syngo.via, picture archiving and communications system software controlled. Intended to be used for viewing, manipulation, communication, and storage of medical images.

Reason

Incorrect values for the volume calculation. Software update VB30B via Update Instructions SY018/16/P to resolve software errors.

Identifiers

code_info
310289,130542,130322,310149,130325,221063,310168,101762,221048,221096,220783,310195,130451,400031,130292,310114,220846,…310289,130542,130322,310149,130325,221063,310168,101762,221048,221096,220783,310195,130451,400031,130292,310114,220846,130269,130163,130402,130826,221051,102336,310282,220888,10007,221052,221049,130518,221002,221091,220915,130520,130472,100469,310249,130122,100013,130378,310188,102453,310079,310080,130240,130382,220985,310171,220879,220995, and 310268.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2245-2016%22

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