BEUDAMED
    FDA Recall Terminated

    Vail 500 Enclosed Bed System.

    Recall: Z-0861-05 · Initiated May 6, 2005

    Recall

    Recall Number
    Z-0861-05
    Event Number
    32055
    Firm
    Vail Products Inc
    FEI Number
    1000122546
    Product Code
    FNL
    Status
    Terminated
    Root Cause
    Device Design
    Initiated
    May 6, 2005
    Posted
    June 30, 2005
    Terminated
    January 5, 2011
    Address
    235 1st St, Toledo, OH, 43605-2041

    Description

    Vail 500 Enclosed Bed System.

    Reason

    Risk of patient entrapment, may result in serious injury or death.

    Action

    The recalling firm sent consignees an urgent notification letter, dated 5/6/05.

    Distribution

    Nationwide, Puerto Rico, Canada and Saudi Arabia. MA, RI, NH, ME, VT, CT, NJ, NY, PA, DE, Washington DC, VA, MD, VA, WV, NC, SC, GA, FL, AL, TN, MS, KY, OH, IN, MI, IA, WI, MN, SD, ND, MT, IL, MO, KS, NE, LA, AR, OK, TX, CO, WY, ID, UT, AZ, NM, NV, CA, HI, OR, WA, and AK.

    Quantity

    345 beds in distribution.