FDA Device recall Z-0956-2023
ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor
- FDA Device
- Class II
- ongoing
- Published 2023-01-25
On 2023-01-25 the FDA classified a Class II recall of ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor by Siemens Medical Solutions Usa, citing mechanical connection between the tabletop and table base may be lost.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0956-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-12-16 |
| Published | 2023-01-25 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor
Reason
Mechanical connection between the tabletop and table base may be lost.
Identifiers
| code_info | 1) ARTIS pheno; Material #10849000; UDI/DI: 4056869046877 2) ARTIS icono biplane; Material #11327600; UDI/DI: 40568690…1) ARTIS pheno; Material #10849000; UDI/DI: 4056869046877 2) ARTIS icono biplane; Material #11327600; UDI/DI: 4056869063317 3) ARTIS icono floor; Material #11327700; UDI/DI: 4056869149325 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0956-2023%22
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