BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NONE

    MDR report key: 1595226 · Received February 2, 2010

    Report

    Report Number
    MW5014628
    Event Type
    Malfunction
    Date Received
    February 2, 2010
    Report Date
    January 27, 2010
    Product Code
    KYX
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NM, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    BISPHENOL A - LISTED AS XENOESTROGENIC AND ESTROGENIC. DATES OF USE: ONGOING. DIAGNOSIS OR REASON FOR USE: PLASTIC BOTTLES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NONE KYX

    Patients

    Seq Age Sex Outcome Treatment
    1 Other