Class II — Siemens Medical Solutions USA, Inc
| Recalling firm | SIEMENS MEDICAL SOLUTIONS USA, INC. |
|---|---|
| Registered facility | View this company's 9 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Software and firmware bugs |
| Product | SOMATOM Force; computed tomography x-ray system. Intended to generate and process cross-sectional images of patients. |
| Quantity | 21 |
| Distribution | Nationwide Distribution |
| Initiated | 2015-08-18 |
| Classified | 2015-10-06 |
| Terminated | 2017-05-08 |
| Recall number | Z-0107-2016 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Siemens Medical Solutions USA, Inc (Z-0107-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/72137/
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