Siemens Artis Q biplane---Interventional Fluoroscopic X-Ray System… — Class II medical device recall Z-1900-2019
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2019-07-10, distributed nationwide. Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potent
| Recall number | Z-1900-2019 |
|---|---|
| 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 | 2019-06-06 |
| Classified | 2019-06-28 |
| Reported by FDA | 2019-07-10 |
| Terminated | 2021-02-09 |
| Distributed | Nationwide (US) |
| Quantity | 73 |
| Serial numbers | 121006, 121013, 121015, 121016, 121020, 121027, 121040, 121049, 121056, 121057, 121058, 121082, 121085, 121089, 121094, 121136, 121137, 121140, 121141, 121144, 121151, 121154, 121155, 121165, 121168 and 47 more |
| Model numbers | 10848282 |
Product
Siemens Artis Q biplane---Interventional Fluoroscopic X-Ray System Model Number: 10848282
Reason for recall
Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off, can result in severe injuries to patients and operating personnel
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-1900-2019. 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.