Artis zee and Artis zeego systems — Class II medical device recall Z-2569-2014
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2014-10-01, distributed nationwide. There is a potential problem with Artis zee and Artis zeego systems running software version VC21B and being u
| Recall number | Z-2569-2014 |
|---|---|
| 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 | 2014-06-05 |
| Classified | 2014-09-22 |
| Reported by FDA | 2014-10-01 |
| Terminated | 2015-04-21 |
| Distributed | Nationwide (US) |
| Quantity | 206 |
| Reason classes | software |
Product
Artis zee and Artis zeego systems. x-ray, angiographic system
Reason for recall
There is a potential problem with Artis zee and Artis zeego systems running software version VC21B and being used in conjunction with the Large Display, in that under certain circumstances, the release of radiation can become blocked unnecessarily.
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-2569-2014. 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.