BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HEARING AID

    MDR report key: 24801587 · Received April 7, 2026

    Report

    Report Number
    MW5186454
    Event Type
    Injury
    Date Received
    April 7, 2026
    Report Date
    April 2, 2026
    Manufacturer
    UNKNOWN
    Product Code
    QUF
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AR, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    PACKAGING, FOUND SCRAPINGS AS WELL AS FRAGMENTS AND VAPE WITH WATER BOTTLE PACKAGING WAS RELABELED. OR LABELED OVER. MARKED FROM (B)(6). REFER TO ADDITIONAL DOCUMENTS IN I2K.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    857257 HEARING AID HEARING AID, AIR-CONDUCTION, OVER THE COUNTER QUF UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Male Other| R| L