BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NEXGEN TAPER STEM PLUG

    MDR report key: 2780664 · Received October 5, 2012

    Report

    Report Number
    1822565-2012-02020
    Event Type
    Injury
    Date Received
    October 5, 2012
    Date of Event
    September 24, 2009
    Report Date
    September 7, 2012
    Manufacturer
    ZIMMER, INC.
    Product Code
    JWH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    EVAL SUMMARY: NEITHER SURGICAL NOTES NOR X-RAYS WERE PROVIDED, THEREFORE FIT AND ORIENTATION COULD NOT BE EVALUATED. PT FACTORS THAT MAY AFFECT THE PERFORMANCE OF THE COMPONENTS SUCH AS BONE QUALITY, ACTIVITY LEVEL OR TYPE OF ACTIVITY (LOW IMPACT VS. HIGH IMPACT) ARE UNK. A DEFINITIVE ROOT CAUSE CANNOT BE DETERMINED WITH THE INFO PROVIDED. MFG DOCUMENTATION FOR THE AVAILABLE LOTS WAS REVIEWED AND INDICATES THAT THE DEVICES WERE MANUFACTURED, INSPECTED, AND PACKAGED TO SPECIFICATION. THERE IS INSUFFICIENT INFO AVAILABLE TO REVIEW RECORDS ON THE TIBIAL PLATE. IT IS NOT SUSPECTED THAT THE PRODUCT FAILED TO MEET SPECIFICATIONS. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY EVIDENCE OF PRODUCT CONTRIBUTION TO THE REPORTED PROBLEM. BASED ON THE AVAILABLE INFO, THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED. SHOULD ADD¿L SUBSTANTIVE INFO BE RECEIVED, THE COMPLAINT WILL BE REOPENED.

    Description of Event or Problem · 1

    IT IS REPORTED THAT THE PT WAS REVISED DUE TO KNEE PAIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NEXGEN TAPER STEM PLUG JWH ZIMMER, INC. 60182485

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention MANUFACTURED BY ZIMMER (B)(4)| NEXGEN MIS MODULAR TIBIAL COMPONENT:| CAT# 00596003702, LOT # UNK| LOT# 60056441| NEXGEN ALL POLY PATELLA: CAT# 00597206532| CAT# 00598009000, LOT# 60175849| NEXGEN STEM EXTENSION REPLACEMENT SCREW: