FDA Device recall Z-0107-2016
SOMATOM Force
- FDA Device
- Class II
- terminated
- Published 2015-10-14
On 2015-10-14 the FDA classified a Class II recall of SOMATOM Force by Siemens Medical Solutions Usa, citing software and firmware bugs.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0107-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-08-18 |
| Published | 2015-10-14 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
SOMATOM Force; computed tomography x-ray system. Intended to generate and process cross-sectional images of patients.
Reason
Software and firmware bugs
Identifiers
| code_info | Model Number of device- 10742326 with serial numbers: 75514 75512 75510 75454 75437 75500 75475 75481 75439…Model Number of device- 10742326 with serial numbers: 75514 75512 75510 75454 75437 75500 75475 75481 75439 75450 75482 75460 75493 75476 75458 75467 75487 75478 75513 75515, and 75501. |
|---|
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-0107-2016%22
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