BEUDAMED
    FDA Enforcement Class II Ongoing

    INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (2019-03-01)

    Recall: Z-0924-2022 · Reported April 20, 2022

    Enforcement

    Recall Number
    Z-0924-2022
    Event ID
    89760
    Classification
    Class II
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Abbott Vascular
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    April 20, 2022
    Initiation Date
    March 11, 2022
    Classification Date
    April 13, 2022
    Address
    26531 Ynez Rd, N/A, Temecula, CA, 92591-4630, United States

    Description

    INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (2019-03-01)

    Reason

    Due to an increase in complaint trend for leaks and intermittent/loose connections.

    Code Info

    Part Numbers: 1000183 Device Identifier-GTIN: 08717648013584 Lot Numbers: 60316775 60322179 60328352 60322176 60326322 60337153

    Distribution

    U.S Nationwide Distribution.: AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, Puerto Rico, SC, TN, TX, VA, WA, and WI. O.U.S.: United Arab Emirates, France, Pakistan, Argentina, United Kingdom, Portugal, Australia, Greece, R¿union, Belgium, Guam, Romania, Brazil, Indonesia, Russian Federation, Bahamas, Israel, Saudi Arabia, Canada, India, Singapore, Switzerland, Italy, Slovakia, Chile, Jamaica, Thailand, China, Japan, Taiwan Republic of China, Colombia, Korea (South), Costa Rica, Luxembourg, Uruguay, Czech Republic, Mexico, Vietnam, Germany, Netherlands, South Africa, Dominican Republic, New Zealand, Spain, and Panama

    Quantity

    6 lots