BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LRG TAP PRI MOD NCK 0DEG 34MM

    MDR report key: 2931203 · Received January 28, 2013

    Report

    Report Number
    0002249697-2013-00329
    Event Type
    Injury
    Date Received
    January 28, 2013
    Date of Event
    January 9, 2013
    Report Date
    January 9, 2013
    Manufacturer
    STRYKER ORTHOPAEDICS-MAHWAH
    Product Code
    MEH
    PMA / PMN Number
    K071082
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    CATALOG NUMBER IS UNKNOWN AT THIS TIME. THE DEVICE WAS REPORTED AS AN UNKNOWN REJUVENATE MODULAR NECK - RIGHT . ADDITIONAL INFORMATION HAS BEEN REQUESTED AND IF RECEIVED, WILL BE PROVIDED IN THE SUPPLEMENTAL REPORT. DEVICE NOT RETURNED TO MANUFACTURER.

    Additional Manufacturer Narrative · 1

    AN EVENT REGARDING UNSPECIFIED SYMPTOMS INVOLVING A REJUVENATE MODULAR DEVICE WAS REPORTED. THE EVENT WAS CONFIRMED. DEVICE EVALUATION WAS NOT PERFORMED AS NO DEVICES WERE RECEIVED. A REVIEW OF DEVICE HISTORY RECORDS FOUND THE DEVICES IN THE REPORTED LOT WERE ACCEPTED INTO FINAL STOCK WITH NO REPORTED DISCREPANCIES. THE SUPER AND CHS COMPLAINT DATABASES SHOW THERE HAVE BEEN OTHER EVENTS FOR THE REPORTED LOT. SIMILAR EVENTS HAVE OCCURRED FOR THE CATALOG NUMBER AND PRODUCT FAMILY. THESE EVENTS WERE DETERMINED TO BE ASSOCIATED WITH RA 2012-067. VOLUNTARY RECALL RA 2012-067 WAS INITIATED FOR ABGII AND REJUVENATE MODULAR STEMS AND NECKS DUE TO THE POTENTIAL RISKS ASSOCIATED WITH THESE DEVICES. THE REPORTED UNSPECIFIED SYMPTOMS IS CONSIDERED TO BE UNDER THE SCOPE OF THIS RECALL. NO FURTHER INVESTIGATION IS REQUIRED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PATIENT IS EXPERIENCING UNSPECIFIED SYMPTOMS. THE FOLLOWING MEASUREMENTS WERE RECORDED AT 28 MONTHS SINCE INDEX SURGERY: COBALT - 9.4; CHROMIUM - 3.4. THIS EVENT DETAILS THE PATIENT'S RIGHT HIP IMPLANTATION. THE PATIENT HAS REJUVENATE MODULAR FEMORAL STEM DEVICES IMPLANTED IN HER LEFT AND RIGHT HIPS.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PATIENT IS EXPERIENCING UNSPECIFIED SYMPTOMS. THE FOLLOWING MEASUREMENTS WERE RECORDED AT 28 MONTHS SINCE INDEX SURGERY: COBALT - 9.4; CHROMIUM - 3.4. THIS EVENT DETAILS THE PATIENT'S RIGHT HIP IMPLANTATION. THE PATIENT HAS REJUVENATE MODULAR FEMORAL STEM DEVICES IMPLANTED IN HER LEFT AND RIGHT HIPS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    37663 LRG TAP PRI MOD NCK 0DEG 34MM IMPLANT MEH STRYKER ORTHOPAEDICS-MAHWAH 29380701

    Patients

    Seq Age Sex Outcome Treatment
    1 Other