ETHICON SUCTION BOVIE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-23 for ETHICON SUCTION BOVIE manufactured by Ethicon Endo-surgery, Inc..

Event Text Entries

[184852116] The cutting function of the ethicon suction bovie did not work. While waiting on someone to deliver a new esu, a new ethicon device was opened which worked. Fda safety report id # (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5093896
MDR Report Key9871629
Date Received2020-03-23
Date of Report2020-03-20
Date of Event2020-03-17
Date Added to Maude2020-03-24
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameETHICON SUCTION BOVIE
Generic NameLAPAROSCOPE, GENERAL & PLASTIC SURGERY
Product CodeGCJ
Date Received2020-03-23
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerETHICON ENDO-SURGERY, INC.


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-23

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