VAPOTHERM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-05-20 for VAPOTHERM manufactured by Vapotherm.

Event Text Entries

[145780464] My mother, (b)(6) who is inpatient and admitted to (b)(6) medical center (b)(6) with pulmonary fibrosis and initially required 100% oxygen was able to improve over the course of 2-3 weeks and was down to 45% oxygen and maintaining sat above 90. On (b)(6) 2019, the vapotherm was beeping for a period of time for no reason. The nurses weren't concerned but after about an hour, pulmonary therapist came in and played with it to get the beeping to stop which it did. However on (b)(6) 2019, the machine malfunctioned and my mother went into respiratory distress until the nurses came in and put her on another form of oxygen until they could get another vapotherm unit. My mother has since struggled to breath and has been increased back to 80% oxygen. Please research. Fda safety report id# (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5086782
MDR Report Key8627756
Date Received2019-05-20
Date of Report2019-05-16
Date of Event2019-05-12
Date Added to Maude2019-05-21
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 FAMILY MEMBER OR FRIEND
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameVAPOTHERM
Generic NameREGULATOR, PRESSURE, GAS CYLINDER
Product CodeCAN
Date Received2019-05-20
Device AvailabilityN
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerVAPOTHERM


Patients

Patient NumberTreatmentOutcomeDate
101. Life Threatening; 2. Required No Informationntervention; 3. Deathisabilit 2019-05-20

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