MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-09-24 for NUBOOM manufactured by Compview Medical.
[21786454]
In our cysto operating room, there are metal and paint chips coming off of the nuboom made by compview medical. Complaints have been made to manufacturer.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5017498 |
| MDR Report Key | 1842637 |
| Date Received | 2010-09-24 |
| Date of Report | 2010-09-24 |
| Date Added to Maude | 2010-10-04 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | NUBOOM |
| Generic Name | NUBOOM |
| Product Code | LMD |
| Date Received | 2010-09-24 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COMPVIEW MEDICAL |
| Manufacturer Address | BEAVERTON OR US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2010-09-24 |