BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    REFOBACIN BONE CEMENT R 40X1

    MDR report key: 6181127 · Received December 16, 2016

    Report

    Report Number
    3006946279-2016-00466
    Event Type
    Malfunction
    Date Received
    December 16, 2016
    Date of Event
    November 16, 2016
    Report Date
    December 15, 2016
    Manufacturer
    BIOMET FRANCE S.A.R.L.
    Product Code
    MBB
    PMA / PMN Number
    PK150850
    Removal / Correction Number
    N/A
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    UDI - (B)(4). CORRECTIVE ACTION HAS BEEN INITIATED FOR THE REPORTED ISSUE.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE STERILE PACKAGE WAS NOT FULLY SEALED. NO PATIENT INVOLVEMENT OR DELAY IN A PROCEDURE WAS REPORTED AS A RESULT OF THE EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    833114 REFOBACIN BONE CEMENT R 40X1 BONE CEMENT, ANTIBIOTIC MBB BIOMET FRANCE S.A.R.L. N/A A606CL0104

    Patients

    Seq Age Sex Outcome Treatment
    1