FDA Device recall Z-1309-2014
Artis Zee Angiographic x-ray systems
- FDA Device
- Class II
- terminated
- Published 2014-04-09
On 2014-04-09 the FDA classified a Class II recall of Artis Zee Angiographic x-ray systems by Siemens Medical Solutions Usa, citing 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 sys….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1309-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-02-07 |
| Published | 2014-04-09 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | AL, AR, MI, MN, NC, NJ, OH, PA, WI |
Product
Artis Zee Angiographic x-ray systems.
Reason
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.
Identifiers
| code_info | Model numbers: 10094135, 10094137, 10094139, 10094141, 10280959. |
|---|
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-1309-2014%22
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