Syngo — Class II medical device recall Z-1705-2015
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2015-06-10, distributed nationwide. measurements drawn on the 2nd and subsequent images of the series are not visible on printouts when the series
| Recall number | Z-1705-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2015-05-15 |
| Classified | 2015-06-03 |
| Reported by FDA | 2015-06-10 |
| Terminated | 2017-03-24 |
| Distributed | Nationwide (US) |
| Quantity | 167 |
| Serial numbers | 100039, 100075, 100220, 100389, 100460, 100484, 100495, 100509, 100530, 100603, 100633, 100662, 100675, 100692, 100700, 100705, 100718, 100729, 100734, 100735, 100742, 100748, 100751, 100753, 100760 and 142 more |
Product
Syngo.via and Syngo.x ; a software solution intended to be used for viewing, manipulation, communication, and storage of medical images.
Reason for recall
measurements drawn on the 2nd and subsequent images of the series are not visible on printouts when the series is sent to print.
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-1705-2015. 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.