LEFT THUMB CONDYLAR IMPLANT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1996-04-22 for LEFT THUMB CONDYLAR IMPLANT manufactured by Unknown.

Event Text Entries

[17896253] Removal of cracked left thumb condylar implant. Device labeled for single use. Patient medical status prior to event: fair condition. 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. Invalid data - regarding whether event presents imminent hazard. 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: none or unknown. Conclusion: none or unknown. Certainty of device as cause of or contributor to event: no. Corrective actions: device permanently removed from service. Invalid data - on device destroyed/disposed of status.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number33156
MDR Report Key33156
Date Received1996-04-22
Date of Report1996-04-22
Date of Event1996-03-28
Date Facility Aware1996-04-09
Report Date1996-04-22
Date Reported to FDA1996-04-22
Date Added to Maude1996-05-17
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 NameLEFT THUMB CONDYLAR IMPLANT
Generic NameCONDYLAR IMPLANT
Product CodeKWG
Date Received1996-04-22
OperatorOTHER CAREGIVERS
Device AvailabilityY
Implant FlagY
Device Sequence No1
Device Event Key34475
ManufacturerUNKNOWN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1996-04-22

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