NeuroLogica Corporation recalls The GC80 Digital X-ray Imaging System
- Recall date
- June 22, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0726-2018
- FDA classification
- Class II
- Brand / firm
- NeuroLogica Corporation
- Sold / distributed
- Nationwide US
Why it was recalled
An image was obtained with over exposure during a Thorax examination using the AEC function.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
The GC80 Digital X-ray Imaging System
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