AMS ACTICON NEOSPHINCTER

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 2014-12-30 for AMS ACTICON NEOSPHINCTER manufactured by American Medical Systems (mn).

Event Text Entries

[21082841] It was reported that the acticon bowel sphincter was removed due to patient dissatisfaction. Another acticon device was implanted. There were no patient complications reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2183959-2014-00579
MDR Report Key4368604
Report Source01,05
Date Received2014-12-30
Date of Report2014-12-11
Date of Event2014-12-04
Date Mfgr Received2014-12-11
Date Added to Maude2014-12-30
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 FDA0
Event Location0
Manufacturer ContactMRS. SHARON ZURN
Manufacturer Street10700 BREN ROAD W
Manufacturer CityMINNETONKA MN 55343
Manufacturer CountryUS
Manufacturer Postal55343
Manufacturer Phone9529306000
Manufacturer G1AMERICAN MEDICAL SYSTEMS (MN)
Manufacturer Street10700 BREN ROAD W
Manufacturer CityMINNETONKA MN 55343
Manufacturer CountryUS
Manufacturer Postal Code55343
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAMS ACTICON NEOSPHINCTER
Generic NameIMPLANTED FECAL INCONTINENCE DEVICE
Product CodeMIP
Date Received2014-12-30
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerAMERICAN MEDICAL SYSTEMS (MN)
Manufacturer Address10700 BREN ROAD W MINNETONKA MN 55343 US 55343


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2014-12-30

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.