MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-12-28 for EGIR WAVEGUIDE 104015 manufactured by Invuity, Inc..
[63399993]
Patient Sequence No: 1, Text Type: N, H10
[63399994]
While surgeon was holding invuity lighted retractor, the plastic light bulb melted in the middle and broke into two pieces.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 6208604 |
| MDR Report Key | 6208604 |
| Date Received | 2016-12-28 |
| Date of Report | 2016-11-23 |
| Date of Event | 2016-11-22 |
| Report Date | 2016-11-23 |
| Date Reported to FDA | 2016-11-23 |
| Date Reported to Mfgr | 2016-11-23 |
| Date Added to Maude | 2016-12-28 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 0 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | EGIR WAVEGUIDE |
| Generic Name | LIGHTED RETRACTOR |
| Product Code | FDG |
| Date Received | 2016-12-28 |
| Model Number | 104015 |
| Lot Number | 16010505 |
| Operator | PHYSICIAN |
| Device Availability | * |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | INVUITY, INC. |
| Manufacturer Address | 444 DE HARO ST. SAN FRANCISCO CA 94107 US 94107 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2016-12-28 |