BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IMP TM 4.1MM MTX FULL,13M

    MDR report key: 7944889 · Received October 8, 2018

    Report

    Report Number
    0002023141-2018-00830
    Event Type
    Malfunction
    Date Received
    October 8, 2018
    Date of Event
    October 23, 2017
    Report Date
    February 18, 2019
    Manufacturer
    ZIMMER DENTAL
    Product Code
    DZE
    PMA / PMN Number
    PK132258
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 0

    NO PRODUCT WAS RETURNED FOR EVALUATION. A DEVICE HISTORY REVIEW WAS PERFORMED AND NO RELATED NONCONFORMANCE¿S WERE NOTED. A COMPLAINT HISTORY SEARCH WAS PERFORMED USING OUR COMPLAINT HANDLING SYSTEM AND THERE WERE NO ADDITIONAL RELATED COMPLAINTS AGAINST THIS LOT. APPROPRIATE DOCUMENTATION WAS REVIEWED. THE ALLEGED MALFUNCTION WAS UNCONFIRMED WITHOUT RETURN OF THE DEVICE. THE REPORTED EVENT COULD NOT RECREATED. BASED ON THE DHR REVIEW, THERE WERE NO MANUFACTURING DEVIATIONS TO SUGGEST THAT THE DEVICE CAUSED OR CONTRIBUTED TO THE REPORTED EVENT. A ROOT CAUSE CANNOT BE DETERMINED.

    Description of Event or Problem · 0

    NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

    Additional Manufacturer Narrative · 1

    ZIMMER BIOMET COMPLAINT (B)(4). ADDITIONAL 510K NUMBERS: K113753 AND K112160. DEVICE NOT RETURNED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE IMPLANT (TMT4B13) FRACTURED. THE IMPLANT WAS NOT REMOVED. NO INJURY TO THE PATIENT RESULTED FROM THE EVENT. TOOTH LOCATION #10.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    783652 IMP TM 4.1MM MTX FULL,13M DENTAL IMPLANT DZE ZIMMER DENTAL 62345414

    Patients

    Seq Age Sex Outcome Treatment
    1 91 YR