BEUDAMED
    FDA Recall Terminated

    Sheridan Sher-I-Bronch Endobronchial Tube for Right Bronchial Intubation; an Rx, sterile, sinlge use endobronchial tube with modified tip for right bronchial intubation, 37 Fr.; Hudson Respiratory Care Inc., Temecula, CA 92589-9020, Manufactured in Mexico; catalog number (REF) 5-16137

    Recall: Z-0681-05 · Initiated February 23, 2005

    Recall

    Recall Number
    Z-0681-05
    Event Number
    31205
    Firm
    Teleflex Medical
    FEI Number
    3004959265
    Product Code
    CBI
    Status
    Terminated
    Root Cause
    Other
    Initiated
    February 23, 2005
    Posted
    April 6, 2005
    Terminated
    July 31, 2006
    Address
    2345 Waukegan Rd, Suite 120, Bannockburn, IL, 60015

    Description

    Sheridan Sher-I-Bronch Endobronchial Tube for Right Bronchial Intubation; an Rx, sterile, sinlge use endobronchial tube with modified tip for right bronchial intubation, 37 Fr.; Hudson Respiratory Care Inc., Temecula, CA 92589-9020, Manufactured in Mexico; catalog number (REF) 5-16137

    Reason

    The distal end of the tube may be printed incorrectly, with catalog numbers V5-16037 and 5-16037 stating 'Bronchial - Right' instead of 'Bronchial - Left', and catalog number 5-16137 stating 'Bronchial - Left' instead of 'Bronchial - Right'.

    Action

    Customers were notified via Federal Express, Next Business Day Delivery, on February 23, 2005. The accounts were informed of the mislabeling and were instructed to inspect the product lots for any incorrectly printed devices, comparing the writing on the sleeve of the blue bronchial tube with the package label which is correct, and to return all identified affected product to Teleflex Medical, Hudson RCI.

    Distribution

    Nationwide and internationally to Argentina, Canada, Chile, China, Costa Rica, Hong Kong, Korea, the Netherlands, South Africa and Vietnam.