WECK HYSTEROSCOPY SCISSORS 150830 UNKNOWN

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1994-08-11 for WECK HYSTEROSCOPY SCISSORS 150830 UNKNOWN manufactured by Linvatec.

Event Text Entries

[20159891] A piece of scissor broke off while instrument being used. Device not labeled for single use. Patient medical status prior to event: unknown. There was not 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. 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, visual examination. Results of evaluation: other. Conclusion: device failure occurred and was related to event. Certainty of device as cause of or contributor to event: yes. Corrective actions: none or unknown. Invalid data - on device destroyed/disposed of status.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9084
MDR Report Key9084
Date Received1994-08-11
Date of Event1993-11-05
Date Facility Aware1993-11-05
Date Added to Maude1994-11-28
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 NameWECK HYSTEROSCOPY SCISSORS
Generic NameSCISSORS
Product CodeHRR
Date Received1994-08-11
Model Number150830
Catalog NumberUNKNOWN
Lot NumberN/A
ID NumberUNKNOWN
OperatorOTHER HEALTH CARE PROFESSIONAL
Device AvailabilityN
Implant FlagN
Device Sequence No1
Device Event Key8744
ManufacturerLINVATEC


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1994-08-11

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