STIMWAVE PNS WIRELESS (STIMQ?)

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-30 for STIMWAVE PNS WIRELESS (STIMQ?) manufactured by Stimwave Technologies Incorp..

Event Text Entries

[177571219] New / worse symptoms; i have received the stimwave wireless pns on (b)(6) 2020 and after anesthesia and pain med wore off become extremely nauseous and vomiting. Rep did not hear of this before. Although online notes, could be caused by over stimulated nerves. Dr told to turn off on wednesday as rep thought it was anesthesia caused. Rep came thursday to reprogram to the lower voltage setting and sent down to program 1. Noticed during program 1, the pain that would normally radiate up to the head and eyeball region would stop at neck and create a new pain in middle of back below the pns implant. Next day - friday night was told to go back to program 2 and within 30 mins nausea and vomiting came back. Went to bed thinking it'll go away and didn't. Rep called again saturday morning and said that he should go back to program 1 at the highest setting and see if that gives enough relief for a permanent implant. Upon waiting until monday's appt to extract the temp leads, the shocking sensations increased and a burning sensation began that became to intense that had to turn off device. The rep appeared to care about the sale and not the actual fact that we should have stopped it at the first sign of nausea after reprogramming. Apparently the rep had never heard of the nausea / vomiting or the burning sensation of where lead placement was and as someone who works in the cro industry i feel that this is something that should be reported as this is a newer device to the market and all ae's should be reported as i feel the rep would not do this. Fda safety report id# (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5092666
MDR Report Key9653796
Date Received2020-01-30
Date of Report2020-01-28
Date of Event2020-01-21
Date Added to Maude2020-01-31
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPATIENT
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTIMWAVE PNS WIRELESS (STIMQ?)
Generic NameSTIMULATOR PERIPHERAL NERVE, IMPLANTED PAIN RELIEF
Product CodeGZF
Date Received2020-01-30
Device AvailabilityN
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerSTIMWAVE TECHNOLOGIES INCORP.


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-30

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