MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1992-08-20 for CMC II COAGULATOR (80-1140) manufactured by Codman & Shurtleff Inc..
[2702]
Patient sustained a lip burn during tonsillectomy. Invalid data - regarding single use labeling of device. Patient medical status prior to event: invalid data. Invalid data - regarding multiple patient involvement. Invalid data - on device service/maintenance. No data - regarding date last serviced. Service provided by: invalid data. Invalid data - service records availability. Invalid data - regarding whether event presents imminent hazard. Invalid data - whether device used as labeled/intended. Invalid data - regarding evaluation by user after event. Method of evaluation: invalid data. Results of evaluation: invalid data. Conclusion: invalid data. Certainty of device as cause of or contributor to event: invalid data. Corrective actions: no data. Invalid data - on device destroyed/disposed of status.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 4466 |
MDR Report Key | 4466 |
Date Received | 1992-08-20 |
Date Added to Maude | 1993-05-25 |
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 | 0 |
Health Professional | 0 |
Initial Report to FDA | 0 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CMC II COAGULATOR (80-1140) |
Product Code | FEH |
Date Received | 1992-08-20 |
Device Availability | * |
Implant Flag | * |
Device Sequence No | 1 |
Device Event Key | 4186 |
Manufacturer | CODMAN & SHURTLEFF INC. |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. No Informationnvalid Deathata | 1992-08-20 |