FDA Device recall Z-1080-2014
Siemens Artis zee Ceiling Systems
- FDA Device
- Class II
- terminated
- Published 2014-03-05
On 2014-03-05 the FDA classified a Class II recall of Siemens Artis zee Ceiling Systems by Siemens Medical Solutions Usa, citing during the lifetime of Artis zee Ceiling systems, there is an increased wear due to potential sub-optimal cable guidance that can lead to cable damage.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1080-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-12-16 |
| Published | 2014-03-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Siemens Artis zee Ceiling Systems. Angiographic x-ray system.
Reason
During the lifetime of Artis zee Ceiling systems, there is an increased wear due to potential sub-optimal cable guidance that can lead to cable damage.
Identifiers
| code_info | Artis zee Ceiling systems serial numbers from 146352 to 147617 |
|---|
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-1080-2014%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.