BEUDAMED
    FDA Adverse Event Other Summary report: N

    INVERNESS EAR PIERCING SYSTEM

    MDR report key: 217702 · Received April 5, 1999

    Report

    Report Number
    2243569-1999-00011
    Event Type
    Other
    Date Received
    April 5, 1999
    Date of Event
    January 22, 1999
    Report Date
    April 5, 1999
    Manufacturer
    INVERNESS CORP.
    Product Code
    JYS
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    SERVICE PERSONNEL

    Narratives

    Description of Event or Problem · 1

    CONSUMER CLAIMS TO HAVE BEEN PIERCED WITH THE INVERNESS EAR PIERCING SYSTEM ON 1/22/99 AT A RETAIL VENDOR. ON 2/23/99, SHE SOUGHT MEDICAL TREATMENT FOR EMBEDMENT OF ONE EARRING AT THE EAR PIERCING SITE. IT WAS REMOVED AND SHE WAS PRESCRIBED ANTIBIOTICS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INVERNESS EAR PIERCING SYSTEM EAR PIERCING INSTRUMENT AND EAR PIERCING EARRINGS JYS INVERNESS CORP. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR Other