BEUDAMED
    FDA Recall Terminated

    Drop Hooks for Xact (tm) Lo-Pro with Removeable Drop Seat, Xact Integrated, and Xact Individual with Integrated Drop Seat wheelchairs, model/item numbers 05D, 1D, and 15D. Packaged as set of four in a poly bag.

    Recall: Z-316/318-3 · Initiated May 14, 2002

    Recall

    Recall Number
    Z-316/318-3
    Event Number
    25070
    Firm
    Action Products Incorporated
    Product Code
    KNO
    Status
    Terminated
    Root Cause
    Other
    Initiated
    May 14, 2002
    Posted
    December 5, 2002
    Terminated
    December 10, 2002
    Address
    22 N Mulberry Street, Hagerstown, MD, 21740

    Description

    Drop Hooks for Xact (tm) Lo-Pro with Removeable Drop Seat, Xact Integrated, and Xact Individual with Integrated Drop Seat wheelchairs, model/item numbers 05D, 1D, and 15D. Packaged as set of four in a poly bag.

    Reason

    Wheelchair seat component is defective.

    Action

    Firm notified customers by certified letter 5/14/02 and advised of potential for serious injury. Letter instructs customers to cease use and distribution of any defective hooks and return for replacement. Firm additonally instructed dealers to notify end-users about the recall.

    Distribution

    Product was sold to medical supply firms in LA, IN, and MA and to international customers.

    Quantity

    73 sets