EVIS EXERA III VIDEO SYSTEM CENTER Adverse Event — Malfunction (MDR 8010047-2020-02411)
EVIS EXERA III VIDEO SYSTEM CENTER Adverse Event — Malfunction (MDR 8010047-2020-02411) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: EVIS EXERA III VIDEO SYSTEM CENTER; Generic name: VIDEO SYSTEM CENTER; Manufacturer: OLYMPUS MEDICAL SYSTEMS CORP..
| Device | EVIS EXERA III VIDEO SYSTEM CENTER |
|---|---|
| Generic name | VIDEO SYSTEM CENTER |
| Manufacturer | OLYMPUS MEDICAL SYSTEMS CORP. |
| Report number | 8010047-2020-02411 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | USER FACILITY |
| Narrative | THIS SUPPLEMENTAL REPORT IS BEING SUBMITTED TO PROVIDE ADDITIONAL INFORMATION AND DEVICE MANUFACTURER DATE. PLEASE SEE THE UPDATES IN SECTIONS: G4, G7, H2, H6, AND H10. THE LEGAL MANUFACTURER REVIEWED THE CONTENT OF THIS COMPLAINT FOR FURTHER INVESTIGATION. THE LEGAL MANUFACTURER REPORTED THAT THE ROOT CAUSE COULD NOT BE DETERMINED. AS THE RESULTS OF THE DHR REVIEW, IT WAS CONFIRMED THAT THERE WAS |
| Source | openFDA MAUDE (device adverse events) |
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