FDA Device recall Z-1469-2017
OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems
- FDA Device
- Class II
- terminated
- Published 2017-03-22
On 2017-03-22 the FDA classified a Class II recall of OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems by Ge Oec Medical Systems, citing OEC FlexiView 8800 workstation power cable assembly issue which can result in a loss of imaging functionality due to intermittent power cord failures.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1469-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-21 |
| Published | 2017-03-22 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Oec Medical Systems |
| Distribution | CA |
Product
OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems
Reason
OEC FlexiView 8800 workstation power cable assembly issue which can result in a loss of imaging functionality due to intermittent power cord failures.
Identifiers
| code_info | OEC FlexiView 8800 systems that had NEMA 5-15 15 Amp power cords replaced between January 28, 2016 and November 23, 2016. |
|---|
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-1469-2017%22
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