FDA Device recall Z-1848-2013
Siemens Luminos dRF Fluoroscopic X-Ray system Fluoroscopic X-Ray system
- FDA Device
- Class II
- terminated
- Published 2013-08-07
On 2013-08-07 the FDA classified a Class II recall of Siemens Luminos dRF Fluoroscopic X-Ray system Fluoroscopic X-Ray system by Siemens Medical Solutions Usa, citing siemens became aware of an unintended behavior when using the Luminos dRF with software version VD10A. The possibility exists that a software error may occur causing the table to….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1848-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-07 |
| Published | 2013-08-07 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | CA, IN, NJ, OK |
Product
Siemens Luminos dRF Fluoroscopic X-Ray system Fluoroscopic X-Ray system
Reason
Siemens became aware of an unintended behavior when using the Luminos dRF with software version VD10A. The possibility exists that a software error may occur causing the table to tilt into an upright position and may collide with the floor. Four consignees were notified of this recall by Update Instruction XP067/12/S -- all four units have been corrected.
Identifiers
| code_info | Model number 10094200, serial numbers 4024, 4077, 4043 and 4051 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1848-2013%22
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