Atlas FDA

syngo Imaging, picture archiving and communications system (PACS), Model number 10 014 063

FDA device recall Z-1235-2009 · posted 2009-04-28 · Terminated

Recall details

Recalling firm
Siemens Medical Solutions USA, Inc
Reason for recall
Incorrect and/or incomplete data: Several potential safety issues while working with the syngo Image product including, but not limited to, data loss, errors in patient data due to different patient IDs, delays in image availability, inaccurate results during image measurements, incorrect review or diagnosis of displayed or printed images, measurement inaccuracies from the host modality and image
Action taken
syngo Imaging has issued an Addendum to the User Manual, which was distributed to affected customers via Update Instructions IM118/08/S in November, 2008. Two safety related hotfixes (VB20G_HF4 and VB30A_HF26) will be released to those affected only after Update Instructions IM118/08/S has been performed. The addendum informs the user about safety relevant notes which pertain to syngo Imaging versions VB20G and VB30A. Update is a prerequisite for the following safety related hotfixes: VB20G_HF4 and VB30A_HF26.
Root cause
Software design
Status
Terminated
Product code
LLZ
Quantity affected
55 units
Distribution
Nationwide Distribution.
Date initiated
2009-01-12
Date posted
2009-04-28
Date terminated
2009-09-23
Location
Malvern, PA

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Related 510(k) clearances

RecordFirmDate
SYNGO IMAGING (VERSION V30) (K071114)Siemens AG Medical Solutions2007-05-22