NX3 Adverse Event — Malfunction (MDR 2024312-2008-00001)
NX3 Adverse Event — Malfunction (MDR 2024312-2008-00001) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: NX3; Generic name: CEMENT, DENTAL; Manufacturer: KERR CORPORATION.
| Device | NX3 |
|---|---|
| Generic name | CEMENT, DENTAL |
| Manufacturer | KERR CORPORATION |
| Report number | 2024312-2008-00001 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Foreign, Health Professional |
| Narrative | IN 2008, A DOCTOR ALLEGED THAT TWO VENEERS PLACED USING NX3 HAD FALLEN OFF. |
| Source | openFDA MAUDE (device adverse events) |
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