FDA Device recall Z-0919-2017
SOMATOM Scope, Computed tomography x-ray system
- FDA Device
- Class II
- terminated
- Published 2017-01-04
On 2017-01-04 the FDA classified a Class II recall of SOMATOM Scope, Computed tomography x-ray system by Siemens Medical Solutions Usa, citing 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 duri….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0919-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-11-22 |
| Published | 2017-01-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | AR, GA, IL, IN, MD, MI, NY, OK, SC, SD |
Product
SOMATOM Scope, Computed tomography x-ray system
Reason
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.
Identifiers
| code_info | Model # 10967666 Serial Number:59376 91766 91767 115456 115454 59380 77560 98840 77557 91758 59377 59378 115451 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0919-2017%22
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