FDA Device recall Z-1490-2017
ONCOR" Avant-garde
- FDA Device
- Class II
- terminated
- Published 2017-03-29
On 2017-03-29 the FDA classified a Class II recall of ONCOR" Avant-garde by Siemens Medical Solutions Usa, citing software update.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1490-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-14 |
| Published | 2017-03-29 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
ONCOR" Avant-garde
Reason
Software update
Identifiers
| code_info | Device Model# 1940035 |
|---|
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-1490-2017%22
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