FDA Device recall Z-2569-2014
Artis zee and Artis zeego systems. x-ray, angiographic system
- FDA Device
- Class II
- terminated
- Published 2014-10-01
On 2014-10-01 the FDA classified a Class II recall of Artis zee and Artis zeego systems. x-ray, angiographic system by Siemens Medical Solutions Usa, citing 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 circ….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2569-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-05 |
| Published | 2014-10-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Artis zee and Artis zeego systems. x-ray, angiographic system
Reason
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.
Identifiers
| code_info | running software version VC21B 10094135, 10094137, 10094141, 10280959 with multiple serial numbers . |
|---|
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-2569-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.