PULSE GEN MODEL 103 Adverse Event — Malfunction (MDR 1644487-2020-00648)
PULSE GEN MODEL 103 Adverse Event — Malfunction (MDR 1644487-2020-00648) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PULSE GEN MODEL 103; Generic name: GENERATOR; Manufacturer: LIVANOVA USA, INC..
| Device | PULSE GEN MODEL 103 |
|---|---|
| Generic name | GENERATOR |
| Manufacturer | LIVANOVA USA, INC. |
| Report number | 1644487-2020-00648 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, CONSUM |
| Narrative | G4, CORRECTED DATA: INITIAL REPORT INADVERTENTLY LISTED 04/03/2020 AS THE DATE RECEIVED BY THE MANUFACTURER, CORRECT DATE IS 04/02/2020. |
| Source | openFDA MAUDE (device adverse events) |
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