GE OEC Medical Systems, Inc recalls OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems
- Recall date
- February 21, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1469-2017
- FDA classification
- Class II
- Brand / firm
- GE OEC Medical Systems, Inc
- Sold / distributed
- One consignee in CA.
Why it was recalled
OEC FlexiView 8800 workstation power cable assembly issue which can result in a loss of imaging functionality due to intermittent power cord failures.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems
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