FDA Device recall Z-1202-2014
Siemens Artis Q and Artis Q biplane systems Product Usage: Interventional Fluoroscopic X-ray
- FDA Device
- Class II
- terminated
- Published 2014-04-02
On 2014-04-02 the FDA classified a Class II recall of Siemens Artis Q and Artis Q biplane systems Product Usage: Interventional Fluoroscopic X-ray by Siemens Medical Solutions Usa, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1202-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-12-05 |
| Published | 2014-04-02 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Siemens Artis Q and Artis Q biplane systems Product Usage: Interventional Fluoroscopic X-ray
Reason
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).
Identifiers
| code_info | model numbers 10848280, 10848281, 10848282, and 10848283. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1202-2014%22
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