Artis zee or Artis Q systems — Class II medical device recall Z-0108-2021
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2020-10-21. Potential exists for the collision supervision not to work properly following loss of the individual room conf
| Recall number | Z-0108-2021 |
|---|---|
| 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 | 2020-08-03 |
| Classified | 2020-10-15 |
| Reported by FDA | 2020-10-21 |
| Terminated | 2021-02-03 |
| Quantity | 124 u.s |
| Serial numbers | 103222, 103285, 103286, 105016, 109016, 109021, 109069, 109105, 109107, 109158, 109163, 109189, 109221, 109300, 109331, 109367, 109371, 109393, 109416, 109451, 109460, 109504, 109505, 109520, 111005 and 99 more |
Product
Artis zee or Artis Q systems (listed below) - Product Usage: for single and biplane diagnostic imaging and interventional procedures. System Name/Material Number: Artis Q BIPLANE 10848282 ARTIS Q CEILING 10848281 Artis Q floor 10848280 ARTIS Q ZEEGO 10848283 ARTIS Q.ZEN BIPLANE 10848355 ARTIS Q.zen ceiling 10848354 Artis Q.zen floor 10848353 Artis zee Biplane 10094141 Artis zee ceiling 10094137 Artis zee floor 10094135 Artis zee floor 10094135 Artis zee multi-purpose 10094139 Artis zeego 10280959
Reason for recall
Potential exists for the collision supervision not to work properly following loss of the individual room configuration data settings causing danger of collision with fix mounted room equipment, walls or floor may occur. This might cause components of the system to fall or tilt which could result in crushing of patients, operators or staff, collision of system parts with patients, as well as result in delay or interruption of the clinical 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-0108-2021. 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.