ROTATABLE SNARE Adverse Event — Injury (MDR 3005099803-2008-00192)
ROTATABLE SNARE Adverse Event — Injury (MDR 3005099803-2008-00192) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ROTATABLE SNARE; Manufacturer: BOSTON SCIENTIFIC CORPORATION; Report number: 3005099803-2008-00192.
| Device | ROTATABLE SNARE |
|---|---|
| Manufacturer | BOSTON SCIENTIFIC CORPORATION |
| Report number | 3005099803-2008-00192 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-22 |
| Report source | Foreign, Health Professional, Company representation |
| Narrative | A ROTATABLE SNARE WAS USED DURING A POLYPECTOMY ON A MALE PT (WEIGHT UNK) IN 2008. ACCORDING TO THE COMPLAINANT, AFTER "A LARGE POLYP WAS REMOVED WITH THIS ROTATABLE SNARE..A SMALL BLEEDING APPEARED". THE TIP OF THE SNARE WAS USED TO COAGULATE THE BLEEDING. REPORTEDLY, AFTER THE COAGULATION, IT WAS DISCOVERED THAT "THE WIRE PARTLY DETACHED FROM [THE TIP OF] THE LOOP." AT THE CONCLUSION OF THE PROC |
| Source | openFDA MAUDE (device adverse events) |
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