BRAVO Adverse Event — Malfunction (MDR 2032545-2008-00732)
BRAVO Adverse Event — Malfunction (MDR 2032545-2008-00732) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BRAVO; Manufacturer: ARIZONA DEVICE MANUFACTURING; Report number: 2032545-2008-00732.
| Device | BRAVO |
|---|---|
| Manufacturer | ARIZONA DEVICE MANUFACTURING |
| Report number | 2032545-2008-00732 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Health Professional |
| Narrative | THE HCP REPORTED THAT WHILE PLACING A BRAVO PH MONITOR THE CAPSULE WOULD NOT ATTACH TO THE PT'S ESOPHAGUS. THE CAPSULE FELL OFF IN THE PT'S MOUTH. NO SERIOUS INJURY TO THE PT WAS REPORTED. |
| Source | openFDA MAUDE (device adverse events) |
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