BEUDAMED
    FDA Enforcement Class II Terminated

    Vista Dental Products Sodium Hypochlorite - 3%, 10 - 12cc Pre-filled Syringes, REF 502315

    Recall: Z-0013-2020 · Reported October 9, 2019

    Enforcement

    Recall Number
    Z-0013-2020
    Event ID
    83435
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Inter-Med Llc
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    October 9, 2019
    Initiation Date
    June 27, 2019
    Classification Date
    October 1, 2019
    Termination Date
    August 10, 2021
    Address
    2200 Northwestern Ave, N/A, Racine, WI, 53404-2500, United States

    Description

    Vista Dental Products Sodium Hypochlorite - 3%, 10 - 12cc Pre-filled Syringes, REF 502315

    Reason

    The affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prolonged storage and exposure to contained solutions, the rubber bung may degrade due to chemical interaction with the bleach solution.

    Code Info

    Lot/Work Order Numbers: 2018-1349 2018-1587 2018-1853 20182107, UDI (01)10818207020427 20182303, UDI (01)10818207020427 20182584, UDI (01)10818207020427 20182666, UDI (01)10818207020427 20190199, UDI (01)10818207020427 20190433, UDI (01)10818207020427

    Distribution

    US, South Africa, Switzerland, Poland, Italy, Singapore, Australia

    Quantity

    582 units