BEUDAMED
    FDA Adverse Event Summary report: N

    THERAFIRM

    MDR report key: 140822 · Received December 30, 1997

    Report

    Report Number
    MW1012698
    Date Received
    December 30, 1997
    Report Date
    December 17, 1997
    Manufacturer
    WARNER-LAMBER CO.
    Product Code
    GAZ
    Report Source
    Voluntary report
    Reporter Location
    VA, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    PHARMACY HAS PARKE-DAVIS THERAFIRM HOSE THAT PARKE DAVIS WILL NOT CREDIT FOR RETURN. THERAFIRM HAS BEEN SWITCHED TO A NEW DIV (SCHOOL CRAFT) AND THEY WILL NOT HONOR ANY RETURN DUE TO THE PARKE-DAVIS LABEL ON THE PRODUCTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 THERAFIRM SURGICAL HOSE GAZ WARNER-LAMBER CO. DIFFERENT SIZES, STYLES. *

    Patients

    Seq Age Sex Outcome Treatment
    1 *