INGEVITY MRI Adverse Event — Malfunction (MDR 2124215-2020-09235)
INGEVITY MRI Adverse Event — Malfunction (MDR 2124215-2020-09235) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INGEVITY MRI; Generic name: IMPLANTABLE LEAD; Manufacturer: BOSTON SCIENTIFIC CORPORATION.
| Device | INGEVITY MRI |
|---|---|
| Generic name | IMPLANTABLE LEAD |
| Manufacturer | BOSTON SCIENTIFIC CORPORATION |
| Report number | 2124215-2020-09235 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | CONSUMER |
| Narrative | AS NO FURTHER INFORMATION CONCERNING THIS REPORT IS EXPECTED, OUR INVESTIGATION IS COMPLETE. THIS INVESTIGATION WILL BE UPDATED SHOULD FURTHER INFORMATION BE PROVIDED. |
| Source | openFDA MAUDE (device adverse events) |
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