FDA Device recall Z-1945-2013
Siemens AXIOM Artis zeego x-ray, angiographic system
- FDA Device
- Class II
- terminated
- Published 2013-08-21
On 2013-08-21 the FDA classified a Class II recall of Siemens AXIOM Artis zeego x-ray, angiographic system by Siemens Medical Solutions Usa, citing siemens issued a customer safety notice about the overlay of system information after a functional check of the brakes on the Artis Zeego system.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1945-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-13 |
| Published | 2013-08-21 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Siemens AXIOM Artis zeego x-ray, angiographic system
Reason
Siemens issued a customer safety notice about the overlay of system information after a functional check of the brakes on the Artis Zeego system.
Identifiers
| code_info | Model number 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-1945-2013%22
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