BEUDAMED
    FDA Recall Terminated

    Line Powered RePak, Model Number 1785S

    Recall: Z-0931-03 · Initiated May 23, 2003

    Recall

    Recall Number
    Z-0931-03
    Event Number
    26330
    FEI Number
    2126518
    Product Code
    GZJ
    Status
    Terminated
    Root Cause
    Other
    Initiated
    May 23, 2003
    Posted
    June 17, 2003
    Terminated
    July 2, 2004
    Address
    Old Hwy 8, Rehabilicare 1811, New Brighton, MN, 55112

    Description

    Line Powered RePak, Model Number 1785S

    Reason

    If there was a short, excessive heat could have been generated in the transformer due to the use of the wrong fuse.

    Action

    Recall letters dated May 21, 2003 requested that consignees return the product and a response form to the firm. Distributors were requested to recall the product from their customers.

    Distribution

    Nationwide in the United States

    Quantity

    618 Line Powered RePaks