Artis zee/ zeego Interventional Fluoroscopic X-Ray System — Class II medical device recall Z-0695-2020
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2019-12-25, distributed in TX, WA. In affected Artis zee floor Interventional Fluoroscopic X-Ray Systems, the activation of a collision sensor wi
| Recall number | Z-0695-2020 |
|---|---|
| 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 | 2019-11-14 |
| Classified | 2019-12-17 |
| Reported by FDA | 2019-12-25 |
| Terminated | 2020-05-12 |
| Distributed | TX, WA |
| Countries outside the US | DK |
| Quantity | 3 |
| Serial numbers | 140422, 140423, 140430 |
| Model numbers | 10094142 |
Product
Artis zee/ zeego Interventional Fluoroscopic X-Ray System, Model Number: 10094142, Software Version: VC21C
Reason for recall
In affected Artis zee floor Interventional Fluoroscopic X-Ray Systems, the activation of a collision sensor will cause a block the movement of the floating tabletop and could result in a delay or interruption of a procedure.
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-0695-2020. 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.