OEC FlexiView 8800 — Class II medical device recall Z-1469-2017
Terminated recall by GE OEC Medical Systems, Inc, reported 2017-03-22, distributed in CA. OEC FlexiView 8800 workstation power cable assembly issue which can result in a loss of imaging functionality
| Recall number | Z-1469-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE OEC Medical Systems, Inc, Salt Lake City, UT, United States |
| Recall initiated | 2017-02-21 |
| Classified | 2017-03-14 |
| Reported by FDA | 2017-03-22 |
| Terminated | 2017-04-24 |
| Distributed | CA |
| Quantity | 1 |
Product
OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems
Reason for recall
OEC FlexiView 8800 workstation power cable assembly issue which can result in a loss of imaging functionality due to intermittent power cord failures.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.