FDA Adverse Event Death Summary report: N

H4I - EUR GP2, UK, AP

MDR report key: 12748120 · Received November 3, 2021

Report

Report Number
3007573469-2021-01120
Event Type
Death
Date Received
November 3, 2021
Date of Event
June 1, 2021
Report Date
July 25, 2022
Manufacturer
RESMED LTD
Product Code
BZD
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
UK
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE STELLAR DEVICE AND H4I HUMIDIFIER WERE RETURNED TO RESMED FOR AN INVESTIGATION. THE INVESTIGATION DETERMINED THAT THERE WAS NO FAULT FOUND WITH THE RETURNED DEVICE. THE DEVICE WAS PERFORMING TO SPECIFICATIONS. RESMED¿S RISK ASSOCIATED WITH USE OF THE DEVICE REMAINS ACCEPTABLE. RESMED REFERENCE #: (B)(4).

Description of Event or Problem · 0

IT WAS REPORTED TO RESMED THAT THE H4I HUMIDIFIER OF A STELLAR WAS USED WITHOUT WATER FILLED BY THE CAREGIVER, THEREFORE ALLEGEDLY DELIVERING DRY AIR TO THE PATIENT WHICH CONTRIBUTED TO RESPIRATORY DETERIORATION AND SUBSEQUENT DEATH OF THE PATIENT. THERE IS NO ALLEGATION OF DEVICE MALFUNCTION.

Additional Manufacturer Narrative · 1

RESMED HAS REQUESTED FOR THE DEVICE TO BE RETURNED SO THAT AN ENGINEERING INVESTIGATION CAN BE PERFORMED. THE DEVICE HAS NOT BEEN RETURNED, THEREFORE RESMED IS UNABLE TO CONFIRM THE ALLEGED MALFUNCTION AT THIS TIME. RESMED REFERENCE #: (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED TO RESMED THAT THE H4I HUMIDIFIER OF A STELLAR WAS USED WITHOUT WATER FILLED BY THE CAREGIVER, THEREFORE ALLEGEDLY DELIVERING DRY AIR TO THE PATIENT WHICH CONTRIBUTED TO RESPIRATORY DETERIORATION AND SUBSEQUENT DEATH OF THE PATIENT. THERE IS NO ALLEGATION OF DEVICE MALFUNCTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1643669 H4I - EUR GP2, UK, AP BZD RESMED LTD 26942

Patients

Seq Age Sex Outcome Treatment
1 15 YR Unknown Death