EMAX 2 PLUS MOTOR Adverse Event — Malfunction (MDR 1045834-2020-00711)
EMAX 2 PLUS MOTOR Adverse Event — Malfunction (MDR 1045834-2020-00711) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: EMAX 2 PLUS MOTOR; Generic name: MOTOR, DRILL, ELECTRIC - HANDPIECE; Manufacturer: DEPUY SYNTHES PRODUCTS LLC.
| Device | EMAX 2 PLUS MOTOR |
|---|---|
| Generic name | MOTOR, DRILL, ELECTRIC - HANDPIECE |
| Manufacturer | DEPUY SYNTHES PRODUCTS LLC |
| Report number | 1045834-2020-00711 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE. ADDITIONAL NARRATIVE: THE ACTUAL DEVICE WAS RETURNED FOR EVALUATION. DURING REPAIR, AN EVALUATION WAS PERFORMED AND IT WAS DETERMINED THAT THE DEVICE FAILED SAFETY ASSESSMENT AND THE CORD WAS DAMAGED. THEREFORE, THE REPORTED CO |
| Source | openFDA MAUDE (device adverse events) |
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