BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PLATE, TIBIAL A/P SLPD OSTEO

    MDR report key: 6300547 · Received February 3, 2017

    Report

    Report Number
    1220246-2017-00009
    Event Type
    Injury
    Date Received
    February 3, 2017
    Date of Event
    June 27, 2017
    Report Date
    February 3, 2017
    Manufacturer
    ARTHREX, INC.
    Product Code
    HRS
    UDI-DI
    00888867009653
    PMA / PMN Number
    K032187
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    PATIENT

    Narratives

    Additional Manufacturer Narrative · 1

    NO FURTHER PATIENT INFORMATION WAS PROVIDED AT THE TIME OF THIS REPORT OR MADE AVAILABLE IN RESPONSE TO FOLLOW-UP COMMUNICATION. NO ADDITIONAL ADVERSE CONSEQUENCES HAVE BEEN REPORTED FROM THIS EVENT. THIS DEVICE IS USED FOR TREATMENT. THE DEVICE WAS REQUESTED FOR EVALUATION BUT WAS NOT RETURNED THEREFORE THE COMPLAINANT'S EVENT COULD NOT BE VERIFIED. THE CAUSE OF THE EVENT COULD NOT BE DETERMINED FROM THE INFORMATION AVAILABLE AND WITHOUT DEVICE EVALUATION. DEVICE HISTORY RECORD REVIEW REVEALED NOTHING RELEVANT TO THIS EVENT. THE MOST LIKELY CAUSE OF THIS EVENT IS FAILURE TO FOLLOW THE POST-OP REHAB PROTOCOL. THE DIRECTIONS FOR USE STATES: POST-OPERATIVELY, UNTIL HEALING IS COMPLETE THE FIXATION PROVIDED BY THIS DEVICE SHOULD BE PROTECTED. THE POSTOPERATIVE REGIMEN PRESCRIBED BY THE PHYSICIAN SHOULD BE STRICTLY FOLLOWED TO AVOID ADVERSE STRESSES APPLIED TO THE IMPLANT. THIS IS THE FIRST COMPLAINT OF THIS TYPE FOR THIS PART/LOT COMBINATION. THE POTENTIAL CAUSE(S) OF THIS EVENT WILL BE COMMUNICATED TO THE FACILITY/SURGEON. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A FOLLOW-UP REPORT WILL BE SUBMITTED. DEVICE REPORTED TO HAVE BEEN DISCARDED.

    Description of Event or Problem · 1

    IT WAS REPORTED BY THE PATIENT THAT HE HAS HAD A FEW REVISION SURGERIES DUE TO SCREWS AND PLATES BREAKING AFTER THE INITIAL KNEE OSTEOTOMY PROCEDURE. ADDITIONAL INFORMATION OBTAINED 1/13/2017 FROM THE SALES REP: PATIENT UNDERWENT A TIBIAL OSTOTOMY PROCEDURE ON (B)(6) 2016 DURING WHICH TIME THE FOLLOWING ARTHREX PRODUCTS WERE IMPLANTED: TIBIAL PLATE AR-13200ST-11.0 LOT 1188334 ((B)(4)), CANCELLOUS SCREW AR-13280-50 (ONE FROM EACH LOT) LOT 1188605 ((B)(4)) AND LOT 1216276 ((B)(4)), CORTICAL SCREW AR-13380-42 LOT 451550 ((B)(4)), CORTICAL SCREW AR-13380-48 LOT 411131 ((B)(4)), OSFERION OSTEO WEDGE AR-13370-3 LOT M13Z06B331 ((B)(4)), AND OSFERION OSTEO WEDGE (QTY 2) AR-13370-2 LOT M14114B344 ((B)(4)). POST SURGERY IT WAS DISCOVERED THAT THE PLATE HAD BROKEN AND ON (B)(6) 2016 THE PATIENT UNDERWENT A REVISION DURING AT WHICH TIME THE ARTHREX PRODUCTS WERE EXPLANTED. TO COMPLETE THE REVISION PROCEDURE THE SURGEON USED A BONE GRAFT WITH AN ANTIBIOTIC IMPREGNATED METHACRYLATE WEDGE. NO ARTHREX PRODUCTS WERE IMPLANTED DURING THE REVISION. THE SURGEON HAD INFORMED THE SALES REP THAT SHE FELT THAT THE CRACKED PLATE MAY HAVE BEEN DUE TO PATIENT NON-COMPLIANCE. ARTHREX WAS ALSO INFORMED THAT THE PATIENT UNDERWENT ANOTHER REVISION SURGERY DURING WHICH ANOTHER MANUFACTURER'S PRODUCT WAS IMPLANTED. THERE WAS NO ARTHREX PRODUCT INVOLVEMENT WITH THE THIRD SURGERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    83551 PLATE, TIBIAL A/P SLPD OSTEO PLATE, FIXATION, BONE HRS ARTHREX, INC. 1188334 00888867009653

    Patients

    Seq Age Sex Outcome Treatment
    1 Other