BEUDAMED
    FDA Adverse Event Death Summary report: N

    REMSTAR PRO CPAP

    MDR report key: 14282536 · Received May 3, 2022

    Report

    Report Number
    MW5109490
    Event Type
    Death
    Date Received
    May 3, 2022
    Report Date
    April 30, 2022
    Manufacturer
    PHILIPS / RESPIRONICS, INC.
    Product Code
    BZD
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MS, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    MY HUSBAND WAS ON THE PHILIPS RESPIRONICS CPAP FOR A COUPLE YEARS. HE WAS DIAGNOSED WITH STAGE 4 ESOPHAGEAL CANCER IN (B)(6) 2012 . HE ULTIMATELY PASSED AWAY IN (B)(6) 2013. FDA SAFETY REPORT ID# (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1378956 REMSTAR PRO CPAP VENTILATOR, NON-CONTINUOUS (RESPIRATOR) BZD PHILIPS / RESPIRONICS, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Male Death