FDA Device recall Z-2219-2012
syngo Dynamics Version 9.5
- FDA Device
- Class II
- terminated
- Published 2012-08-29
On 2012-08-29 the FDA classified a Class II recall of syngo Dynamics Version 9.5 by Siemens Medical Solutions Usa, citing if multiple uncompressed images/clips are sent to the syngo Dynamics server, around the same time, it is possible for an image from a patient to be placed in another patient's stu….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2219-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-07-13 |
| Published | 2012-08-29 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
syngo Dynamics Version 9.5
Reason
If multiple uncompressed images/clips are sent to the syngo Dynamics server, around the same time, it is possible for an image from a patient to be placed in another patient's study.
Identifiers
| code_info | 10091862 and 10091863 |
|---|
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-2219-2012%22
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