REVEAL XT Adverse Event — Malfunction (MDR 9614453-2020-01357)
REVEAL XT Adverse Event — Malfunction (MDR 9614453-2020-01357) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: REVEAL XT; Generic name: DETECTOR AND ALARM, ARRHYTHMIA; Manufacturer: MEDTRONIC EUROPE SARL.
| Device | REVEAL XT |
|---|---|
| Generic name | DETECTOR AND ALARM, ARRHYTHMIA |
| Manufacturer | MEDTRONIC EUROPE SARL |
| Report number | 9614453-2020-01357 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
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