NURO 3533

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2017-03-01 for NURO 3533 manufactured by Advanced Uro-solutions, L.l.c..

Event Text Entries

[68748345] A good faith effort will be made to obtain the applicable information relevant to the report. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[68748346] A patient reported that since starting the therapy their left leg had been bothering them with muscle spasms. It was the same leg they were getting treatment on. They noted they had neuropathy since 1999 and believed that the treatment had been aggravating it. It was hard for them to get out of bed. The patient also mentioned they had a revision on their knee. They spoke to their healthcare provider about the issues and the hcp stated that it had nothing to do with the treatments, so they would try to administer the treatment to patients other leg. The patient was concerned about that option because they had ruptured that achilles heel and had screws in place and didn't want any further problems. After starting the treatments, the patient also reported they had to wait 5-10 minutes before they can void. Sometimes when they push, they feel like their straining which is not good, the urine should just come out. After the first treatment, they could not void. They had no urge to go, and they did not feel their bladder full either. That seemed abnormal to the patient because they consumed a lot of caffeine and water to be able to go to the bathroom. They also felt as though they were off balance as though they may fall. They advised that they almost fell on top of their spouse a couple of week prior to the report. Their hcp stated that was odd and to monitor it. The patient now walks with a cane, since starting treatments, which the hcp was aware of. The patient also noted that they had problems with their lowerback and had a morphine pump that was prior to the treatments. The patient had completed 4 sessions total.
Patient Sequence No: 1, Text Type: D, B5


[70579852] (b)(4) is no longer applicable to this event.
Patient Sequence No: 1, Text Type: N, H10


[110478326] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3012165443-2017-00009
MDR Report Key6369169
Report SourceCONSUMER
Date Received2017-03-01
Date of Report2017-03-22
Date of Event2017-02-07
Date Mfgr Received2017-03-22
Date Added to Maude2017-03-01
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 FDA3
Event Location3
Manufacturer ContactLISA CLARK
Manufacturer Street7000 CENTRAL AVENUE NE RCW215
Manufacturer CityMINNEAPOLIS MN 55432
Manufacturer CountryUS
Manufacturer Postal55432
Manufacturer Phone7635263920
Manufacturer G1ADVANCED URO-SOLUTIONS, L.L.C.
Manufacturer Street7842 HICKORY FLAT HIGHWAY SUITE D
Manufacturer CityWOODSTOCK GA 30188
Manufacturer CountryUS
Manufacturer Postal Code30188
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNURO
Generic NameSTIMULATOR,PERIPHERAL NERVE,NON-IMPLANTED,FOR PELVIC FLOOR DYSFUNCTION
Product CodeNAM
Date Received2017-03-01
Model Number3533
Catalog Number3533
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerADVANCED URO-SOLUTIONS, L.L.C.
Manufacturer Address7842 HICKORY FLAT HIGHWAY SUITE D WOODSTOCK GA 30188 US 30188


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-03-01

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