FDA Device recall Z-2128-2020
Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194
- FDA Device
- Class II
- terminated
- Published 2020-06-03
On 2020-06-03 the FDA classified a Class II recall of Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194 by Siemens Medical Solutions Usa, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2128-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-04-17 |
| Published | 2020-06-03 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194
Reason
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.
Identifiers
| code_info | Serial Numbers: 50135 50131 50171 50129 50048 50184 50180 50136 50185 50153 50155 50130 50127 50134 50166 50192 50161 50128 50132 50160 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2128-2020%22
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