BEUDAMED
    FDA Recall Terminated

    Channel Neuroendoscope, Standard Resolution, 13 cm, Catalog No. 2232-003.

    Recall: Z-0050-04 · Initiated September 15, 2003

    Recall

    Recall Number
    Z-0050-04
    Event Number
    27299
    Firm
    Medtronic Neurosurgery
    FEI Number
    3015531529
    Product Code
    GWG
    Status
    Terminated
    Root Cause
    Labeling mix-ups
    Initiated
    September 15, 2003
    Posted
    July 20, 2004
    Terminated
    October 21, 2003
    Address
    125 Cremona Drive, Goleta, CA, 93117

    Description

    Channel Neuroendoscope, Standard Resolution, 13 cm, Catalog No. 2232-003.

    Reason

    Size mix-up. 13 cm product may be labeled as 21.6 mm and visaversa.

    Action

    Firm sales representatives will contact customers and hand deliver the recall notice.

    Distribution

    TN, CO, GA and Japan

    Quantity

    10