FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: syngo X Workplace is a medical workstation for real-time viewing, image manipulation, 3D-visualization, communication, and storage of medical images and data on exchange media. It is used for diagnostic image viewing and post processing during interventional procedures. .
- Recall number
- Z-1232-2016
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- syngo X Workplace is a medical workstation for real-time viewing, image manipulation, 3D-visualization, communication, and storage of medical images and data on exchange media. It is used for diagnostic image viewing and post processing during interventional procedures. .
- Status
- Terminated
- Initiated
- 2016-02-24
- Posted
- 2016-03-23
- Terminated
- 2017-02-16
- Reason
- After importing, the segmentation results appear mirrored at the CARTO system and can't be used for the ablation procedure.
- Root cause
- Software design
- Action
- Siemens sent an Important Customer Safety Notice dated February 24, 2016, to all affected customers notifying them that the issue will be remedied with a software update via AX004/16/S. Following the installation of this update, the segmentation results can be used at the CARTO system as described in the operator manual. Customers with questions were instructed to call 800-888-7436. For questions regarding this recall call 610-448-6461.
- Quantity
- 6
- Distribution
- Nationwide Distribution to IL, NY, MT, and MN.
- Lot, serial or model codes
- Serial # 20119, 20098, 20041, 20124, 12177, 20026
- 510(k) numbers
- ["K143319"]
- PMA numbers
- not on file
- Product code
- LLZ
- Firm FEI
- 2240869
- Firm city
- Malvern
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28