CONTINUOUS EPIDURAL CATH 8024-05

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1993-01-06 for CONTINUOUS EPIDURAL CATH 8024-05 manufactured by Abbott Laboratories.

Event Text Entries

[22071671] Seperated - portion left in patient surgically removedinvalid 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. No imminent hazard to public health claimed. 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


MAUDE Entry Details

Report Number4396
MDR Report Key4396
Date Received1993-01-06
Date of Report1993-01-06
Date of Event1992-09-18
Report Date1993-01-06
Date Reported to FDA1993-01-06
Date Added to Maude1993-05-21
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 NameCONTINUOUS EPIDURAL CATH
Product CodeGBQ
Date Received1993-01-06
Model Number8024-05
OperatorOTHER HEALTH CARE PROFESSIONAL
Device Availability*
Implant Flag*
Device Sequence No1
Device Event Key4121
ManufacturerABBOTT LABORATORIES


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 1993-01-06

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