RADIAL JAW 4 Adverse Event — Report (MDR 10004672)
RADIAL JAW 4 Adverse Event — Report (MDR 10004672) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: RADIAL JAW 4; Generic name: FORCEPS, BIOPSY, ELECTRIC; Manufacturer: BOSTON SCIENTIFIC CORPORATION.
| Device | RADIAL JAW 4 |
|---|---|
| Generic name | FORCEPS, BIOPSY, ELECTRIC |
| Manufacturer | BOSTON SCIENTIFIC CORPORATION |
| Report number | 10004672 |
| Product problem | N |
| Date received | 2020-04-28 |
| Narrative | THE SURGEON STATED THAT THE CLAMP/ JAW PORTION OF THE FORCEPS BENT WHILE INSIDE OF THE PATIENT, THE FORCEPS AND ENDOSCOPE WAS THEN REMOVED FROM THE PATIENT. THE CLAMP/ JAW OF THE FORCEPS HAD TO BE BROKEN IN ORDER TO REMOVE THE DEVICE FROM THE ENDOSCOPE. |
| Source | openFDA MAUDE (device adverse events) |
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