ELEVATE PROLAPSE REPAIR SYSTEM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,04 report with the FDA on 2013-01-03 for ELEVATE PROLAPSE REPAIR SYSTEM manufactured by American Medical Systems, Inc..

Event Text Entries

[3063644] It was reported by the plaintiff's attorney that the plaintiff was implanted with a elevate on or about (b)(6) 2004. It was reported by the plaintiff's attorney that the plaintiff experienced emotional distress and a problem with the product. The device was implanted for treatment.
Patient Sequence No: 1, Text Type: D, B5


[10366550] Should additional information become available regarding this event it will be re-evaluated and a follow-up report will be sent as appropriate. Lawyer-filed report-(b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2183959-2013-00003
MDR Report Key2901106
Report Source00,04
Date Received2013-01-03
Date of Report2012-11-19
Date Mfgr Received2012-12-07
Date Added to Maude2013-01-09
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 FDA0
Event Location0
Manufacturer ContactSHARON ZURN, DIRECTOR
Manufacturer Street10700 BREN RD., WEST
Manufacturer CityMINNETONKA MN 55343
Manufacturer CountryUS
Manufacturer Postal55343
Manufacturer Phone9529306347
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameELEVATE PROLAPSE REPAIR SYSTEM
Generic NameSURGICAL MESH
Product CodeOPT
Date Received2013-01-03
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerAMERICAN MEDICAL SYSTEMS, INC.
Manufacturer Address10700 BREN RD., WEST MINNETONKA MN 55343 US 55343


Patients

Patient NumberTreatmentOutcomeDate
101. Deathisabilit 2013-01-03

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