Artis Zee Angiographic x-ray systems — Class II medical device recall Z-1309-2014
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2014-04-09, distributed in AL, AR, MI, MN, NC, NJ, OH, PA…. An inappropriate cable connection was assembled for certain Artis zee systems. which may cause a system failur
| Recall number | Z-1309-2014 |
|---|---|
| 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 | 2014-02-07 |
| Classified | 2014-03-31 |
| Reported by FDA | 2014-04-09 |
| Terminated | 2015-03-16 |
| Distributed | AL, AR, MI, MN, NC, NJ, OH, PA, WI |
| Quantity | 9 |
| Model numbers | 10094135, 10094137, 10094139, 10094141, 10280959 |
Product
Artis Zee Angiographic x-ray systems.
Reason for recall
An inappropriate cable connection was assembled for certain Artis zee systems. which may cause a system failure and possibly lead to a restricted maneuverability of the gantry system.
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-1309-2014. 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.