Artis zee systems x-ray — Class II medical device recall Z-0172-2014
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2013-11-20, distributed in AR, AZ, CA, CT, FL, IA, KS, KY…. The firm became aware of a potential issue with Artis zee systems bearing model numbers 10094135, 10094137, an
| Recall number | Z-0172-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2013-01-21 |
| Classified | 2013-11-14 |
| Reported by FDA | 2013-11-20 |
| Terminated | 2014-10-29 |
| Distributed | AR, AZ, CA, CT, FL, IA, KS, KY, MO, MT, NY, OK, PA, WV |
| Quantity | 17 |
| Model numbers | 10094135, 10094137, 10094141 |
Product
Artis zee systems x-ray, angiographic system
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0172-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.