Siemens Artis Q and Artis Q biplane systems Product Usage:… — Class II medical device recall Z-1202-2014
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2014-04-02, distributed nationwide. There exists the possibility that during clinical operation, a breakdown of the x-ray tube could result in los
| Recall number | Z-1202-2014 |
|---|---|
| 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 | 2013-12-05 |
| Classified | 2014-03-27 |
| Reported by FDA | 2014-04-02 |
| Terminated | 2014-11-06 |
| Distributed | Nationwide (US) |
| Quantity | 19 |
| Model numbers | 10848280, 10848281, 10848282, 10848283 |
Product
Siemens Artis Q and Artis Q biplane systems Product Usage: Interventional Fluoroscopic X-ray
Reason for recall
There exists the possibility that during clinical operation, a breakdown of the x-ray tube could result in loss of x-ray imaging for the Artis Q and Artis Q biplane systems with a flat detector as 40 HDR (large 30x40).
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-1202-2014. 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.