FDA Device recall Z-2078-2012
Siemens syngo.plaza
- FDA Device
- Class II
- terminated
- Published 2012-08-01
On 2012-08-01 the FDA classified a Class II recall of Siemens syngo.plaza by Siemens Medical Solutions Usa, citing siemens became aware of a potential malfunction when using syngo.plaza with software version VA20C_HF01. For datasets with distance measurements it can happen, that all images are….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2078-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-02-24 |
| Published | 2012-08-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Siemens syngo.plaza. Radiological image processing system
Reason
Siemens became aware of a potential malfunction when using syngo.plaza with software version VA20C_HF01. For datasets with distance measurements it can happen, that all images are not loaded to Viewer but no error message is displayed to user.
Identifiers
| code_info | Model number 10592457 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2078-2012%22
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