SYNTHETIC SLING/MESH 72403281 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2002-06-14 for SYNTHETIC SLING/MESH 72403281 NA manufactured by American Medical Systems, Inc..

Event Text Entries

[17514993] Infection/pain - sling explanted. Info received late.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2183959-2002-00030
MDR Report Key399503
Report Source05
Date Received2002-06-14
Date of Report2002-06-12
Date of Event2001-09-25
Date Mfgr Received2002-06-11
Date Added to Maude2002-06-18
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactTHERESE BOWKER, MDR CONTACT
Manufacturer Street10700 BREN ROAD WEST
Manufacturer CityMINNETONKA MN 55343
Manufacturer CountryUS
Manufacturer Postal55343
Manufacturer Phone9529306624
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSYNTHETIC SLING/MESH
Generic NameSURGICAL MESH
Product CodeFHK
Date Received2002-06-14
Model Number72403281
Catalog NumberNA
Lot NumberNI
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeNA
Device Eval'ed by MfgrN
Implant FlagY
Date RemovedM
Device Sequence No1
Device Event Key388554
ManufacturerAMERICAN MEDICAL SYSTEMS, INC.
Manufacturer Address10700 BREN RD WEST MINNETONKA MN 55343 US
Baseline Brand NameSYNTHETIC SLING/MESH
Baseline Generic NameSURGICAL MESH
Baseline Model No72403281
Baseline Catalog NoNA
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2002-06-14

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