LAPAROSCOPIC TROCAR SLEEVE W/CLIP VALVE 8351.07

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1993-11-10 for LAPAROSCOPIC TROCAR SLEEVE W/CLIP VALVE 8351.07 manufactured by Richard Wolf Gmbh.

Event Text Entries

[16365488] During a laparoscopic procedure, a small section of material broke off of the fiberglass tip. Two (2) pieces approx. 1 x 10 mm each were retreived from patient's abdomen. No other problems were reported. Invalid data - regarding single use labeling of device. Patient medical status prior to event: unknown. 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: 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 Number1418479-1993-09002
MDR Report Key7105
Date Received1993-11-10
Date of Report1993-09-15
Date of Event1993-08-23
Date Facility Aware1993-09-03
Report Date1993-09-15
Date Reported to FDA1993-09-15
Date Reported to Mfgr1993-09-15
Date Added to Maude1993-12-09
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationUNKNOWN
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameLAPAROSCOPIC TROCAR SLEEVE W/CLIP VALVE
Generic NameLAPAROSCOPIC TROCAR SLEEVE
Product CodeFBQ
Date Received1993-11-10
Model Number8351.07
Catalog Number8351.07
Lot NumberM-F-R
OperatorOTHER HEALTH CARE PROFESSIONAL
Device Availability*
Implant Flag*
Device Sequence No1
Device Event Key6787
ManufacturerRICHARD WOLF GMBH


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1993-11-10

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