NEXGEN OSCILLATOR BLADE, BRAZOL COATED Adverse Event — Malfunction (MDR 1017294-2008-00109)
NEXGEN OSCILLATOR BLADE, BRAZOL COATED Adverse Event — Malfunction (MDR 1017294-2008-00109) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: NEXGEN OSCILLATOR BLADE, BRAZOL COATED; Generic name: OSCILLATING BLADE, 19.5 X 86 X 1.27MM; Manufacturer: CONMED LINVATEC.
| Device | NEXGEN OSCILLATOR BLADE, BRAZOL COATED |
|---|---|
| Generic name | OSCILLATING BLADE, 19.5 X 86 X 1.27MM |
| Manufacturer | CONMED LINVATEC |
| Report number | 1017294-2008-00109 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-14 |
| Report source | Foreign, Health Professional, User facility |
| Narrative | THE SURGEON REPORTED, THAT DURING USE OF THIS BLADE IN A TOTAL KNEE SURGERY, THE TEETH AND HUB BROKE. TO DATE, THERE IS NO REPORT OF INJURY ASSOCIATED WITH THIS EVENT. |
| Source | openFDA MAUDE (device adverse events) |
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