MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2003-11-13 for ENDOSTAT * manufactured by *.
[17374832]
Laser fiber tip defective & broke off in pt's airway - able to retrieve w/ forceps.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 528880 |
| MDR Report Key | 528880 |
| Date Received | 2003-11-13 |
| Date of Report | 2003-09-27 |
| Date of Event | 2003-09-16 |
| Date Reported to FDA | 2003-09-30 |
| Date Added to Maude | 2004-06-10 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ENDOSTAT |
| Generic Name | * |
| Product Code | HPJ |
| Date Received | 2003-11-13 |
| Model Number | * |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | * |
| Device Age | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 518068 |
| Manufacturer | * |
| Manufacturer Address | * * * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2003-11-13 |