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 |