FDA Device recall Z-0048-2013
Siemens syngo.plaza radiological image processing system
- FDA Device
- Class II
- terminated
- Published 2012-10-17
On 2012-10-17 the FDA classified a Class II recall of Siemens syngo.plaza radiological image processing system by Siemens Medical Solutions Usa, citing siemens became aware of an unintended behavior when using syngo.plaza. In syngo.plaza within the online "Short Time Storage" (STS), some studies are marked with an archived icon,….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0048-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-06-06 |
| Published | 2012-10-17 |
| 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 an unintended behavior when using syngo.plaza. In syngo.plaza within the online "Short Time Storage" (STS), some studies are marked with an archived icon, however, the entry in the Archive Database referring to the physical file may be missing.
Identifiers
| code_info | Model number 10592457, serial numbers 100263, 100401, 100177, 100138, 100174, 100406, 100249, 100201, 100198, 100181, 100146. |
|---|
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-0048-2013%22
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