BEUDAMED
    FDA Recall Terminated

    Shower Seat, Non-rotating, Catalog number 727152000

    Recall: Z-0464-2010 · Initiated July 9, 2009

    Recall

    Recall Number
    Z-0464-2010
    Event Number
    53161
    Firm
    Nutech Manufacturing Corp
    FEI Number
    3006525314
    Product Code
    IKX
    Status
    Terminated
    Root Cause
    Device Design
    Initiated
    July 9, 2009
    Posted
    December 1, 2009
    Terminated
    May 29, 2013
    Address
    2024 Broad Street PO Box 840, Pocomoke City, MD, 21851-0840

    Description

    Shower Seat, Non-rotating, Catalog number 727152000

    Reason

    Safety chair used in shower/bath may not meet specifications for weight load.

    Action

    The subsidiary distributor, Maddak, Inc. notified customers by A "Voluntary Product Recall Notice", phone and e-mail on 07/09/2009. The own label distributor instructed customers to return their inventory of affected products received between May 1, 2009 and July 7, 2009. Distributors were instructed to immediately quarantine then return all affected inventory to Maddak and notify their accounts. Distributors were requested to instruct dealers to display a "storefront" notice and provide consumers with a customer response form. Distributors were also requested to forward a request to dealers to post a website notice if they have one. Recovered products will be replaced.

    Distribution

    Worldwide Distribution -- USA and Canada.

    Quantity

    3,627 total units