BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BIPAP AUTO SERIES ASSY

    MDR report key: 13957783 · Received March 31, 2022

    Report

    Report Number
    2518422-2022-09424
    Event Type
    Malfunction
    Date Received
    March 31, 2022
    Date of Event
    March 5, 2018
    Report Date
    August 29, 2025
    Manufacturer
    RESPIRONICS, INC
    Product Code
    BZD
    PMA / PMN Number
    K091319
    Removal / Correction Number
    RES 88058
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    HK
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    THIS MDR IS BEING SUBMITTED AS PART OF A BATCH SUBMISSION OF COMPLAINTS THAT WERE REASSESSED AS REPORTABLE FOAM DEGRADATION COMPLAINTS; DISCOVERED AS PART OF A RETROSPECTIVE REMEDIATION REVIEW.

    Additional Manufacturer Narrative · 0

    THE MANUFACTURER PREVIOUSLY REPORTED THAT REQUIRED INTERVENTION TO PREVENT PERMANENT IMPAIRMENT/DAMAGE, OCCURED IN SECTION B2. AFTER REVIEW, IT WAS DETERMINED THAT THIS OPTION WAS INCORRECTLY SELECTED IN SECTION B2. NOTHING SUCH HAS OCCURED TO THE PATIENT. THE REPORT SHOULD HAVE BEEN SENT FOR PRODUCT PROBLEM ONLY IN SECTION B1. IN H6 TYPE OF INVESTIGATION CODE WAS MISSING. IN G4 SECTION PMA/510(K) NUMBER WAS INCORRECT THE CORRECT VALUE IS K050759.

    Description of Event or Problem · 0

    THE MANUFACTURER RECEIVED INFORMATION ALLEGING AN ISSUE RELATED TO A BIPAP DEVICE'S SOUND ABATEMENT FOAM. THERE WAS NO REPORT OF PATIENT HARM OR INJURY. THIS ISSUE WAS REPORTED TO THE FDA PER 21 CFR 806. THE DEVICE WILL BE CORRECTED PER RES 88058.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1108110 BIPAP AUTO SERIES ASSY VENTILATOR, NON-CONTINUOUS (RESPIRATOR) BZD RESPIRONICS, INC 751P

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention