PULSE GEN MODEL 105 Adverse Event — Injury (MDR 1644487-2020-00628)
PULSE GEN MODEL 105 Adverse Event — Injury (MDR 1644487-2020-00628) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PULSE GEN MODEL 105; Generic name: GENERATOR; Manufacturer: LIVANOVA USA, INC..
| Device | PULSE GEN MODEL 105 |
|---|---|
| Generic name | GENERATOR |
| Manufacturer | LIVANOVA USA, INC. |
| Report number | 1644487-2020-00628 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | EXPLANTED GENERATOR IS BEING RETURNED FOR PRODUCT ANALYSIS. EXPLANTED PRODUCT HAS NOT BEEN RECEIVED TO DATE. |
| Source | openFDA MAUDE (device adverse events) |
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