FDA Device recall Z-0465-2013
Siemens syngo.plaza Radiological Image Processing System Usage: Radiological Image Processing System
- FDA Device
- Class II
- terminated
- Published 2012-12-12
On 2012-12-12 the FDA classified a Class II recall of Siemens syngo.plaza Radiological Image Processing System Usage: Radiological Image Processing System by Siemens Medical Solutions Usa, citing firm has become aware of an unintended behavior when using syngo.plaza and issued an Update Instruction. The Update Instruction SY050/12/S provides a software update and addresses….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0465-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-06-20 |
| Published | 2012-12-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Siemens syngo.plaza Radiological Image Processing System Usage: Radiological Image Processing System
Reason
Firm has become aware of an unintended behavior when using syngo.plaza and issued an Update Instruction. The Update Instruction SY050/12/S provides a software update and addresses the following issues: - Patient Rename messages for the same patient are being continually processed for several days. This fills up the 'pcvdbsrv' log and potentially affects performance of the system. - Data could
Identifiers
| code_info | Model number 10 592 457 |
|---|
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-0465-2013%22
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