FDA Device recall Z-1354-2015
Syngo.plaza
- FDA Device
- Class II
- terminated
- Published 2015-04-08
On 2015-04-08 the FDA classified a Class II recall of Syngo.plaza by Siemens Medical Solutions Usa, citing possibly incomplete archived studies during pre-fetch. In a server farm setup, when pre-fetch/retrieve operation is performed for partially archived studies, the series that have….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1354-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-02-18 |
| Published | 2015-04-08 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | FL, MA, WI |
Product
Syngo.plaza. A Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in diagnosis and treatment planning.
Reason
Possibly incomplete archived studies during pre-fetch. In a server farm setup, when pre-fetch/retrieve operation is performed for partially archived studies, the series that have not yet been archived, will remain unarchived.
Identifiers
| code_info | Model Numbers of device: 10592457, 10863172, serial numbers: 100177 100033 100181 100029 |
|---|
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-1354-2015%22
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