ARTIS pheno — Class II medical device recall Z-0956-2023
Ongoing recall by Siemens Medical Solutions USA, Inc, reported 2023-01-25, distributed nationwide. Mechanical connection between the tabletop and table base may be lost.
| Recall number | Z-0956-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2022-12-16 |
| Classified | 2023-01-13 |
| Reported by FDA | 2023-01-25 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, BG, CA, CH, CL, CN, CO, CZ, DE, DK, EG, ES, FI, FR, GB, GR, HK, ID, IE, IN, IR, IT, JP, KR, KW, LB, NL, NO, NZ, OM, PL, QA, SA, SE, SG, SK, TH, TW, VN, ZA |
| Quantity | 550 units |
| UPC / GTIN / UDI-DI | 04056869046877, 04056869063317, 04056869149325 |
Product
ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor
Reason for recall
Mechanical connection between the tabletop and table base may be lost.
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-0956-2023. 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.