PRECAUTIONS OF USING THE STERILIZATION CAP Adverse Event — Injury (MDR 8010047-2020-02393)
PRECAUTIONS OF USING THE STERILIZATION CAP Adverse Event — Injury (MDR 8010047-2020-02393) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PRECAUTIONS OF USING THE STERILIZATION CAP; Generic name: STERILIZATION CAP; Manufacturer: OLYMPUS MEDICAL SYSTEMS CORP..
| Device | PRECAUTIONS OF USING THE STERILIZATION CAP |
|---|---|
| Generic name | STERILIZATION CAP |
| Manufacturer | OLYMPUS MEDICAL SYSTEMS CORP. |
| Report number | 8010047-2020-02393 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | USER FACILITY |
| Narrative | THIS SUPPLEMENTAL REPORT IS BEING SUBMITTED TO PROVIDE ADDITIONAL INFORMATION. THE DEVICE WAS NOT RETURNED TO OLYMPUS MEDICAL SYSTEMS CORP. (OMSC), THEREFORE OMSC CANNOT INVESTIGATE THE SUBJECT DEVICE. OMSC REVIEWED THE MANUFACTURING HISTORY (DHR) OF THE SUBJECT DEVICE AND CONFIRMED NO IRREGULARITY. THE EXACT CAUSE OF THE REPORTED EVENT COULD NOT BE CONCLUSIVELY DETERMINED. IF ADDITIONAL INFORMATI |
| Source | openFDA MAUDE (device adverse events) |
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