FDA Device recall Z-2472-2018
SOMATOM Emotion 6 (Model 10165888)
- FDA Device
- Class II
- terminated
- Published 2018-08-08
On 2018-08-08 the FDA classified a Class II recall of SOMATOM Emotion 6 (Model 10165888) by Siemens Medical Solutions Usa, citing A potential risk of unnecessary radiation exposure due to a software issue.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2472-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-02-01 |
| Published | 2018-08-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
SOMATOM Emotion 6 (Model 10165888)
Reason
A potential risk of unnecessary radiation exposure due to a software issue
Identifiers
| code_info | Serial No. 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 1016588…Serial No. 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 |
|---|
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-2472-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.