BEUDAMED
    FDA Recall Terminated

    KayserBetten model IDA beds Product Usage: BED, AC-POWERED ADJUSTABLE HOSPITAL

    Recall: Z-0522-2014 · Initiated April 11, 2013

    Recall

    Recall Number
    Z-0522-2014
    Event Number
    65915
    Firm
    mobility unlimited inc
    FEI Number
    3006791363
    Product Code
    FNL
    Status
    Terminated
    Root Cause
    Device Design
    Initiated
    April 11, 2013
    Posted
    December 17, 2013
    Terminated
    October 8, 2014
    Address
    515 N 12th St, Allentown, PA, 18102-2755

    Description

    KayserBetten model IDA beds Product Usage: BED, AC-POWERED ADJUSTABLE HOSPITAL

    Reason

    Some joints on the doors of a limited number of IDA beds may loosen or separate over time which can cause the doors to drop outward and cause injury.

    Action

    Mobility Unlimited sent a notification letters dated April 12, 2013 to affected customers The letter identified the affected product, problem and actions to be taken. The letter informed customers that a Retrofit Kits along with illustrated instructions will be sent. For questions call 1-800-574-7880.

    Distribution

    Worldwide Distribution - USA Nationwide in the states of AL, AZ, CA, FL, GA, IL, MN, MO, NY, PA, TN, TX, VA, and Canada.

    Quantity

    33 beds