Artis zeego — Class II medical device recall Z-1343-2022
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2022-07-13, distributed nationwide. It may occur that after system startup no stand movement is possible any longer in the event of a discharged B
| Recall number | Z-1343-2022 |
|---|---|
| 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 | 2022-05-24 |
| Classified | 2022-07-07 |
| Reported by FDA | 2022-07-13 |
| Terminated | 2025-01-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, CA, CH, CN, DE, FI, FR, GB, HK, IN, IT, JP, KR, LB, LT, LU, NL, PL, PT |
| UPC / GTIN / UDI-DI | 04056869010007, 04056869010083 |
| Model numbers | 10280959, 10848283 |
Product
Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopic X-Ray System
Reason for recall
It may occur that after system startup no stand movement is possible any longer in the event of a discharged BIOS battery of the robotic stand control PC. If this problem occurs during startup, all stand movements are blocked and can only be reactivated by a field service engineer.
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-1343-2022. 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.