syngo Dynamics Version 9 — Class II medical device recall Z-2219-2012
Terminated recall by Siemens Medical Solutions, USA, Inc, reported 2012-08-29, distributed nationwide. If multiple uncompressed images/clips are sent to the syngo Dynamics server, around the same time, it is possi
| Recall number | Z-2219-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions, USA, Inc, Ann Arbor, MI, United States |
| Recall initiated | 2012-07-13 |
| Classified | 2012-08-17 |
| Reported by FDA | 2012-08-29 |
| Terminated | 2013-07-15 |
| Distributed | Nationwide (US) |
| Quantity | 30 |
Product
syngo Dynamics Version 9.5
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2219-2012. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.