NUPULSE NDU

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-16 for NUPULSE NDU manufactured by Nupulse Cv, Inc..

Event Text Entries

[183517537] Rn was in pt's room and heard alarm sounding. Nupulse was not inflating and deflating at this time, rn called charge rn. Np was also called to bedside. Alarm on screen was "attention (4). Battery fault. " per nupulse binder, external battery was changed. Device still not functioning with battery exchange. Pt was switched to back up navigation distribution unit. Nupulse now functioning at this time. Pt asymptomatic throughout. Upon assessment, battery life was 6 hrs and 21 mins, external battery was 97% and internal battery was 91% charged. Nupulse hotline called and updated. Rns advised to contact research team- called and aware. She will bring pt's discharge kit with backup navigation distribution unit to bedside tomorrow am. For tonight, md brought back up ndu slated for or case tomorrow.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9835251
MDR Report Key9835251
Date Received2020-03-16
Date of Report2020-03-06
Date of Event2020-01-28
Report Date2020-03-06
Date Reported to FDA2020-03-06
Date Reported to Mfgr2020-03-16
Date Added to Maude2020-03-16
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Generic NameNUPULSE NDU
Product CodeKMA
Date Received2020-03-16
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerNUPULSE CV, INC.
Manufacturer Address5734 TRINITY ROAD SUITE 101 RALEIGH NC 27607 US 27607


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-16

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