Home / Recalls / Siemens Medical Solutions USA, Inc / Z-2477-2018

Z-2477-2018 Class II Terminated

Recalled by Siemens Medical Solutions USA, Inc — Malvern, PA

FDA device recall Z-2477-2018 was initiated by Siemens Medical Solutions USA, Inc on Feb 1, 2018 and is designated Class II. Reason for recall: A potential risk of unnecessary radiation exposure due to a software issue The recall status is terminated (terminated May 1, 2020).

Recall Details

Product Type: Devices
Report Date: Aug 8, 2018
Initiation Date: Feb 1, 2018
Termination Date: May 1, 2020
Voluntary/Mandated: Voluntary: Firm initiated

Product Description

SOMATOM Scope Power (Model 10967888)

Reason for Recall

A potential risk of unnecessary radiation exposure due to a software issue

Distribution Pattern

Nationwide

Code Information

Serial No. 99329 98809 98886 99041 91203 91342 91475 98908 99019 99199 99248 99278 91286 98840 90872 90811 91486 98925 99049 91176 90939 91417 99258 91206 99296 91201 99295 99004 98991 90916 91090 99305 99179 91213 91402 91196 99244 90942 91133 91393 91506 99110 91494 91132 91204 98807 98875 99015 91418 91474 91108 91178 98926 91057 91179 91360 91367 99150 91310 91473 91396 99111 91263 91543 91190 91191 90907 91265 91416 99127 99255 99018 91355 91419 98814 91369 91222 91291 99274 99005 91376 91081 98855 91264 98788 90906 91325 91256 91038

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-2477-2018
openFDA file date: Oct 26, 2026
Loaded by RegDataLab: Oct 27, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.