VESICA PERC STABILIZATION KIT WITH PROTEGEN SLING UNK

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2004-03-11 for VESICA PERC STABILIZATION KIT WITH PROTEGEN SLING UNK manufactured by Boston Scientific Corp..

Event Text Entries

[354982] It was reported that subsequent to the implant of a protegen sling for treatment in 1998. The pt began experiencing infections and erosion through vaginal wall in september of 2003. The sling was removed in 2003. Pt returned to experiencing incontinence.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number6000043-2004-00015
MDR Report Key515383
Report Source05,06
Date Received2004-03-11
Date Added to Maude2004-03-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactNANCY CUTINO
Manufacturer StreetONE BOSTON SCIENTIFIC PLACE
Manufacturer CityNATICK MA 01760153
Manufacturer CountryUS
Manufacturer Postal01760153
Manufacturer Phone5086525066
Manufacturer G1BOSTON SCIENTIFIC
Manufacturer Street780 BROOKSIDE DRIVE
Manufacturer CitySPENCER IN 47460
Manufacturer CountryUS
Manufacturer Postal Code47460
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVESICA PERC STABILIZATION KIT WITH PROTEGEN SLING
Generic NamePERC STABILIZATION KIT
Product CodeFHK
Date Received2004-03-11
Model NumberNA
Catalog NumberUNK
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeNA
Device Eval'ed by MfgrR
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key504391
ManufacturerBOSTON SCIENTIFIC CORP.
Manufacturer Address780 BROOKSIDE DR. SPENCER IN 47460 US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2004-03-11

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