SOMATOM Scope Power — Class II medical device recall Z-0920-2017
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2017-01-04, distributed in AR, GA, IL, IN, MD, MI, NY, OK…. Siemens is providing a new installation of the Residual Current Monitor (RCM) in the Line Connection Box (LCB)
| Recall number | Z-0920-2017 |
|---|---|
| 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 | 2016-11-22 |
| Classified | 2016-12-23 |
| Reported by FDA | 2017-01-04 |
| Terminated | 2017-05-30 |
| Distributed | AR, GA, IL, IN, MD, MI, NY, OK, SC, SD |
| Serial numbers | 115451, 115454, 115456, 59376, 59377, 59378, 59380, 77557, 77560, 91758, 91766, 91767, 98840 |
| Model numbers | 10967888 |
Product
SOMATOM Scope Power, Computed tomography x-ray system
Reason for recall
Siemens is providing a new installation of the Residual Current Monitor (RCM) in the Line Connection Box (LCB) to resolve a potential defect that could lead to a power cutout during use of the SOMATOM Scope, Scope Power and Perspective systems.
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-0920-2017. 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.