BEUDAMED
    FDA Enforcement Class II Terminated

    Ferno PROFlexx¿ Model 28Z Chair Cot

    Recall: Z-1827-2017 · Reported April 26, 2017

    Enforcement

    Recall Number
    Z-1827-2017
    Event ID
    76765
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Ferno-Washington Inc
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    E-Mail
    Report Date
    April 26, 2017
    Initiation Date
    March 8, 2017
    Classification Date
    April 15, 2017
    Termination Date
    June 29, 2017
    Address
    70 Weil Way, N/A, Wilmington, OH, 45177-9371, United States

    Description

    Ferno PROFlexx¿ Model 28Z Chair Cot

    Reason

    The recall was initiated as a result of the detection of an incorrect nut used in manufacturing.

    Code Info

    17E003185, 17E003169, 17E003179, 17E003180, 17E003181, 17E003183, 17E003187, 17E003152, 17E003168, 17E003171, 17E003172, 17E003173, 17E003184, 17E003170, 17E003138, 17E003139, 17E003140, 17E003141, 17E003153, 17E003154, 17E003155, 17E003156, 17E003157, 17E003158, 17E003159, 17E003160, 17E003161, 17E003162, 17E003163, 17E003164, 17E003165, 17E003166, 17E003167, 17E003174

    Distribution

    Worldwide distribution. The recalled products were distributed to the following states: CA, FL, HI, IL, NY, OH. There are no government accounts for this recall. There are no Canada accounts for this recall. There are no Mexico accounts for this recall. The recalled product was distributed to the following countries: Taiwan, United Arab Emirates, Thailand, Singapore

    Quantity

    34 units