WALKAIDE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2008-09-02 for WALKAIDE manufactured by Innovative Neurotronics.

Event Text Entries

[932225] This patient uses the walkaide device from innovative neurotronics which is a device that uses skin surface electrodes to treat drop foot. Patient's father e-mailed on 08/27/2008 stating that the patient had developed sores on her leg at the electrode sites, which took approximately one month to heal. Patient has not been wearing the walkaide since the sores developed. I have not seen the patient since the sores developed. We are currently trying to schedule for follow up. Dates of use: 2008. Diagnosis or reason for use: drop foot, traumatic brain injury. Event abated after use stopped or dose reduced: yes. The walkaide was delivered to the patient in 2008. I do not know when the device was discontinued, however, the father stated in his e-mail that the patient stopped using the device about one month prior to sending the 08/27/2008 e-mail notifying me that the patient had developed sores.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5008165
MDR Report Key1146184
Date Received2008-09-02
Date of Report2008-09-02
Date of Event2008-07-28
Date Added to Maude2008-09-09
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameWALKAIDE
Generic NameWALKAIDE
Product CodeGZI
Date Received2008-09-02
OperatorLAY USER/PATIENT
Device AvailabilityY
Implant FlagN
Date RemovedB
Device Sequence No1
Device Event Key1166404
ManufacturerINNOVATIVE NEUROTRONICS
Manufacturer AddressBETHESDA MD US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2008-09-02

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