AMS SPHINCTER 800 URINARY PROSTHESIS AUS

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 2012-01-25 for AMS SPHINCTER 800 URINARY PROSTHESIS AUS manufactured by American Medical Systems, Inc..

Event Text Entries

[2555762] On (b)(6) 2007 pt was implanted with aus device. On (b)(6) 2011 ams was notified that the physician "added 2nd cuff. " ams clarified the reason for the addition of a cuff. On (b)(6) 2011 ams received a response "i believe it was cuff atrophy. " the device was patent and "working but not closing off completely. "
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2183959-2012-00081
MDR Report Key2431151
Report Source05
Date Received2012-01-25
Date of Report2011-09-27
Date of Event2011-08-10
Date Mfgr Received2011-09-27
Date Added to Maude2012-01-31
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 ContactJON CORNELL, SR. MANAGER
Manufacturer Street10700 BREN ROAD WEST
Manufacturer CityMINNETONKA MN 55343
Manufacturer CountryUS
Manufacturer Postal55343
Manufacturer Phone9529306670
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAMS SPHINCTER 800 URINARY PROSTHESIS
Generic NameARTIFICIAL URINARY SPHINCTER
Product CodeFAG
Date Received2012-01-25
Model NumberAUS
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerAMERICAN MEDICAL SYSTEMS, INC.
Manufacturer Address10700 BREN ROAD WEST MINNETONKA MN 55343 US 55343


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2012-01-25

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