Cios Spin Image-Intensified Fluoroscopic X-Ray System — Class II medical device recall Z-2128-2020
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2020-06-03, distributed nationwide. The unplugging of the main cable on the monitor trolley from the X10 connector can cause an unsafe electrical
| Recall number | Z-2128-2020 |
|---|---|
| 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 | 2020-04-17 |
| Classified | 2020-05-26 |
| Reported by FDA | 2020-06-03 |
| Terminated | 2020-08-25 |
| Distributed | Nationwide (US) |
| Quantity | 20 |
| Serial numbers | 50048, 50127, 50128, 50129, 50130, 50131, 50132, 50134, 50135, 50136, 50153, 50155, 50160, 50161, 50166, 50171, 50180, 50184, 50185, 50192 |
| Model numbers | VA30-10308194 |
Product
Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194
Reason for recall
The unplugging of the main cable on the monitor trolley from the X10 connector can cause an unsafe electrical voltage (up to 67,6 V DC) at the X10 connector. This can result in an electrical shock if the user or other persons touch the contact pins of the X10 connector.
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-2128-2020. 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.