BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ PASS 70 DEGREE LEFT

    MDR report key: 7235682 · Received February 2, 2018

    Report

    Report Number
    0001825034-2018-00661
    Event Type
    Malfunction
    Date Received
    February 2, 2018
    Report Date
    February 14, 2018
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    HWQ
    PMA / PMN Number
    PN/A
    Removal / Correction Number
    N/A
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(6). CONCOMITANT: 904054, EZ PASS 70 DEGREE LEFT, 256930; 904054, EZ PASS 70 DEGREE LEFT, 256930. CUSTOMER HAS INDICATED THAT THE PRODUCT IS IN PROCESS OF BEING RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 - 2018 - 00660, 0001825034 - 2018 - 00659.

    Additional Manufacturer Narrative · 1

    (B)(4) UPON REASSESSMENT OF THE REPORTED EVENT, IT WAS DETERMINED THAT THE INFORMATION PROVIDED ON THIS FORM WAS PREVIOUSLY SUBMITTED UNDER MANUFACTURING REPORT NUMBER 0001825034 - 2018 - 00372.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE NITINOL WIRE WOULD NOT SCROLL OUT OF THE PASSER SHAFT. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    80052 EZ PASS 70 DEGREE LEFT PASSER HWQ ZIMMER BIOMET, INC. N/A 256930

    Patients

    Seq Age Sex Outcome Treatment
    1