BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CORAIL2 NON COL HO SIZE 18

    MDR report key: 4241951 · Received November 10, 2014

    Report

    Report Number
    1818910-2014-31489
    Event Type
    Injury
    Date Received
    November 10, 2014
    Date of Event
    February 5, 2014
    Report Date
    October 17, 2014
    Manufacturer
    DEPUY FRANCE S.A.S.-SAINT PRIEST - 3003895575
    Product Code
    KWA
    PMA / PMN Number
    PK042992
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.THE ASR PLATFORM WAS VOLUNTARILY RECALLED FROM THE MARKET IN AUGUST 2010, AND THE ASR PRODUCT CODES ARE NOW CONSIDERED INACTIVE. FURTHER INVESTIGATION OF THIS INDIVIDUAL INCIDENT WILL NOT BE UNDERTAKEN, AS THERE IS AN ONGOING INVESTIGATION REGARDING THE ROOT CAUSE(S) AND/OR CORRECTIVE ACTIONS. (B)(4). DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT AND/OR ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED.(B)(4).

    Description of Event or Problem · 1

    SALES REP REPORTED REVISION SURGERY. PATIENT HAS BEEN REVISED TO ADDRESS PAIN, ELEVATED METAL ION LEVELS AND PSEUDOTUMOR. SALES REP ALSO NOTED THAT PATIENT IS SUING. LEGAL CLAIM RECEIVED 1/20/2014. UPDATE REC¿D 5/15/2014 - LITIGATION RECEIVED. LITIGATION ALLEGES DISCOMFORT AND WEAKNESS. THERE IS NO NEW ADDITIONAL INFORMATION THAT WOULD AFFECT THE INVESTIGATION. THIS COMPLAINT WAS UPDATED ON: 06/05/2014. UPDATE REC¿D 10/15/2014 - PLAINTIFF¿S PRELIMINARY DISCLOSURE FORM WAS RECEIVED, WHICH IDENTIFIED DOB INFORMATION. THE STEM AND SLEEVE ARE BEING ADDED TO THE COMPLAINT. THE COMPLAINT AND ASSOCIATED MDRS WERE UPDATED. THERE WAS NO NEW INFORMATION THAT WOULD CHANGE THE OUTCOME OF THE INVESTIGATION. THE COMPLAINT WAS UPDATED ON: 11/10/2014.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    723955 CORAIL2 NON COL HO SIZE 18 HIP FEMORAL STEM/SLEEVE KWA DEPUY FRANCE S.A.S.-SAINT PRIEST - 3003895575 2462069

    Patients

    Seq Age Sex Outcome Treatment
    1 45 YR Required Intervention