U.S. ENDOSCOPY Adverse Event — Malfunction (MDR MW5005569)
U.S. ENDOSCOPY Adverse Event — Malfunction (MDR MW5005569) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: U.S. ENDOSCOPY; Generic name: CAPSULE DELIVERY DEVICE; Manufacturer: U.S. ENDOSCOPY.
| Device | U.S. ENDOSCOPY |
|---|---|
| Generic name | CAPSULE DELIVERY DEVICE |
| Manufacturer | U.S. ENDOSCOPY |
| Report number | MW5005569 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-01-18 |
| Narrative | DR. PUT CAPSULE IN DELIVERY DEVICE. CAPSULE IN DEVICE WAS FINE UNTIL ATTEMPT MADE TO GO THROUGH PYLORUS TO DELIVER CAPSULE TO THE DUODENUM. THE END OF THE DELIVERY DEVICE CAME OFF WITH CAPSULE IN DEVICE. CAPSULE AND DEVICE RETRIEVAL WITH ROTH BAI KIT. DATE OF USE: 2008. |
| Source | openFDA MAUDE (device adverse events) |
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