VOCARE BLADDER SYSTEM 1904 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 2003-03-19 for VOCARE BLADDER SYSTEM 1904 NA manufactured by Neurocontrol Corp..

Event Text Entries

[15714326] Patient was implanted with vocare bladder system in 2000. On january 22, 2003 the vocare bladder system stopped working. Patient was using catheterization for voiding. 2 months later surgery was performed and the entire device was replaced as the fault in the implant was close to the spine. The patient is now using the new device. This report is considered complete and no follow-up report is anticipated.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1530440-2003-00004
MDR Report Key448981
Report Source05
Date Received2003-03-19
Date of Event2003-02-21
Date Mfgr Received2003-02-21
Date Added to Maude2003-03-24
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 Location0
Manufacturer ContactKATHIE MIZAK
Manufacturer Street8333 ROCKSIDE ROAD
Manufacturer CityVALLEY VIEW OH 44125
Manufacturer CountryUS
Manufacturer Postal44125
Manufacturer Phone2169120101
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVOCARE BLADDER SYSTEM
Generic NameSACRAL ANTERIOR ROOT STIMULATOR FOR BLADDER/BOWEL
Product CodeGZC
Date Received2003-03-19
Model Number1904
Catalog NumberNA
Lot NumberNA
ID NumberNA
OperatorLAY USER/PATIENT
Device Eval'ed by Mfgr*
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key437965
ManufacturerNEUROCONTROL CORP.
Manufacturer Address8333 ROCKSIDE RD VALLEY VIEW OH 44125 US
Baseline Brand NameVOCARE BLADDER SYSTEM
Baseline Generic NameSACRAL ANTERIOR ROOT STIMULATOR FOR BLADDER/BOWEL
Baseline Model No1904
Baseline Catalog NoNA
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2003-03-19

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.