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 04 report with the FDA on 2003-06-04 for VOCARE BLADDER SYSTEM 1904 NA manufactured by Neurocontrol Corp.

Event Text Entries

[273631] Initial report involved an external equipment problem. External equipment was ruled out as the problem. It is thought that there may be a loose connection with the receiver or other internal problem. Revision surgery is tentatively scheduled and a follow up report will be submitted once the revision surgery is performed.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1530440-2003-00007
MDR Report Key463580
Report Source04
Date Received2003-06-04
Date of Report2003-06-04
Date of Event2003-05-05
Date Mfgr Received2003-05-05
Date Added to Maude2003-06-05
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 STIMULATION FOR BLADDER/BOWEL
Product CodeGZC
Date Received2003-06-04
Model Number1904
Catalog NumberNA
Lot NumberNA
ID NumberNA
OperatorLAY USER/PATIENT
Device Availability*
Device Eval'ed by Mfgr*
Implant FlagY
Date RemovedA
Device Sequence No1
Device Event Key452522
ManufacturerNEUROCONTROL CORP
Manufacturer Address8333 ROCKSIDE RD VALLEY VIEW OH 441256104 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 2003-06-04

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