FDA Device recall Z-0172-2014
Artis zee systems x-ray, angiographic system
- FDA Device
- Class II
- terminated
- Published 2013-11-20
On 2013-11-20 the FDA classified a Class II recall of Artis zee systems x-ray, angiographic system by Siemens Medical Solutions Usa, citing the firm became aware of a potential issue with Artis zee systems bearing model numbers 10094135, 10094137, and 10094141 equipped with a card collimator from a specific lot where….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0172-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-01-21 |
| Published | 2013-11-20 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | AR, AZ, CA, CT, FL, IA, KS, KY, MO, MT, NY, OK, PA, WV |
Product
Artis zee systems x-ray, angiographic system
Reason
The firm became aware of a potential issue with Artis zee systems bearing model numbers 10094135, 10094137, and 10094141 equipped with a card collimator from a specific lot where a dislocation of the scatter radiation filter inside the card collimator may occur.
Identifiers
| code_info | model numbers 10094135, 10094137, and 10094141 equipped with a card collimator from a specific lot |
|---|
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-0172-2014%22
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