BEUDAMED
    FDA Adverse Event Other Summary report: N

    PLAYTEX NURSER DELUXE DOUBLE ELECTRIC BREAST PUMP

    MDR report key: 3724160 · Received March 31, 2014

    Report

    Report Number
    MW5035426
    Event Type
    Other
    Date Received
    March 31, 2014
    Date of Event
    March 27, 2014
    Report Date
    March 28, 2014
    Product Code
    HGX
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    RECEIVED NOTICE OF A RECALL ON THE BREAST PUMP: (B)(6) 2014 ENERGIZER PERSONAL CARE PLAYTEX MANUFACTURING, INC. ANNOUNCED TODAY IT IS INITIATING A VOLUNTARY NATIONWIDE RECALL OF CERTAIN AC/DC POWER ADAPTERS THAT ARE USED WITH THE PLAYTEX NURSER DELUXE DOUBLE ELECTRIC BREAST PUMP. CONSUMER SAFETY IS A PRIMARY OBJECTIVE OF PLAYTEX AND WE ARE TAKING THIS ACTION OUT OF AN ABUNDANCE OF CAUTION. THE CAUSING ON SOME ADAPTERS MAY BECOME LOOSE AND SEPARATE, RESULTING IN A POTENTIAL FOR ELECTRIC SHOCK. NO INJURIES HAVE BEEN REPORTED TO DATE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    189743 PLAYTEX NURSER DELUXE DOUBLE ELECTRIC BREAST PUMP PLAYTEX NURSER DELUXE DOUBLE ELECTRIC BREAST PUMP HGX

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR