HEARTMATE 3 LVAS IMPLANT KIT Adverse Event — Injury (MDR 2916596-2020-02095)
HEARTMATE 3 LVAS IMPLANT KIT Adverse Event — Injury (MDR 2916596-2020-02095) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: HEARTMATE 3 LVAS IMPLANT KIT; Generic name: VENTRICULAR (ASSISST) BYPASS; Manufacturer: THORATEC CORPORATION.
| Device | HEARTMATE 3 LVAS IMPLANT KIT |
|---|---|
| Generic name | VENTRICULAR (ASSISST) BYPASS |
| Manufacturer | THORATEC CORPORATION |
| Report number | 2916596-2020-02095 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | NO FURTHER INFORMATION WAS PROVIDED. A SUPPLEMENTAL REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER¿S INVESTIGATION IS COMPLETED. |
| Source | openFDA MAUDE (device adverse events) |
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