BEUDAMED
    FDA Adverse Event Injury Summary report: N

    STRYKER ENDOSCOPY

    MDR report key: 358123 · Received October 23, 2001

    Report

    Report Number
    MW1023180
    Event Type
    Injury
    Date Received
    October 23, 2001
    Date of Event
    October 16, 2001
    Report Date
    October 23, 2001
    Manufacturer
    STRYKER ENDOSCOPY
    Product Code
    HRX
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PT HAD A LEFT KNEE ARTHROSOCPY WITH AN ACC RECONSTRUCTION. AFTER PROCEDURE COMPLETED DR FELT PT HAD DEVELOPED COMPARTMENT SYNDROME REQUIRING A FASCIOTOMY. STRYKER ARTHROSCOPY PUMP WAS USED DURING CASE. SURGEON FELT PRESSURE READING NOT TO BE CORRECT. ARTHROSCOPY PUMP SENT TO STRYKER FOR EVALUATION. SALES REP NOTIFIED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    47642 STRYKER ENDOSCOPY ARTHOSCOPY PUMP HRX STRYKER ENDOSCOPY * *

    Patients

    Seq Age Sex Outcome Treatment
    1 21 YR Required Intervention