ELECTROSURGICAL GENERATOR 9600 N/A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1992-10-08 for ELECTROSURGICAL GENERATOR 9600 N/A manufactured by Concept, Inc..

Event Text Entries

[617] During excision of a basal cell carcinoma with skin flap to right cheek, the electrosurgical generator ignited the drapes on the patient's face. The patient was stabilized and the surgery was completed without incidentdevice not labeled for single use. Patient medical status prior to event: satisfactory condition. There was not multiple patient involvement. Device serviced in accordance with service schedule. Date last serviced: 01-may-92. Service provided by: user facility biomedical/bioengineering department. Service records available. No imminent hazard to public health claimed. Device used as labeled/intended. Device was evaluated after the event. Method of evaluation: actual device involved in incident was evaluated, electrical tests performed, performance tests performed, visual examination. Results of evaluation: none or unknown. Conclusion: none or unknown. Certainty of device as cause of or contributor to event: invalid data. Corrective actions: device temporarily removed from service. Invalid data - on device destroyed/disposed of status.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1745
MDR Report Key1745
Date Received1992-10-08
Date of Report1992-09-14
Date of Event1992-09-03
Date Facility Aware1992-09-03
Report Date1992-09-14
Date Reported to FDA1992-09-14
Date Reported to Mfgr1992-09-04
Date Added to Maude1992-11-19
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameELECTROSURGICAL GENERATOR
Generic NameN/A
Product CodeFAR
Date Received1992-10-08
Model Number9600
Catalog NumberN/A
Lot NumberN/A
ID Number002148
OperatorOTHER HEALTH CARE PROFESSIONAL
Device AvailabilityY
Device Age01-DEC-87
Implant FlagN
Device Sequence No1
Device Event Key1648
ManufacturerCONCEPT, INC.


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 1992-10-08

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