BEUDAMED
    FDA Recall Terminated

    Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.

    Recall: Z-2753-2018 · Initiated November 3, 2017

    Recall

    Recall Number
    Z-2753-2018
    Event Number
    80556
    Firm
    Handicare Usa Inc
    FEI Number
    3007802293
    Product Code
    FNL
    Status
    Terminated
    Root Cause
    Nonconforming Material/Component
    Initiated
    November 3, 2017
    Terminated
    July 10, 2020
    Address
    10888 Metro Ct, Maryland Heights, MO, 63043-2413

    Description

    Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.

    Reason

    Premature strap wear and breakage at maximum weight conditions (625 lbs.).

    Action

    HandiCare USA sent an Urgent notification letter dated November 3, 2017 to their customers. The letter identified the affected product, problem and actions to be taken. Customers were informed new units will be sent to replace the affected units identified at no charge. For questions contact your Customer Service

    Distribution

    Worldwide Distribution - US Nationwide in the states of AK, CA, CT, DE, GA, IA, IL, KY, LA, MA, ME, MI, MN, MO, NE, NV, NY, OH, OR, PA, RI, TN, TX, WI, and Puerto Rico and the countries of Canada and Australia,

    Quantity

    4