BEUDAMED
    FDA Enforcement Class II Completed

    IceRod" 1.5 i-Thaw" Cryoablation Needle

    Recall: Z-0665-2021 · Reported December 30, 2020

    Enforcement

    Recall Number
    Z-0665-2021
    Event ID
    86777
    Classification
    Class II
    Status
    Completed
    Product Type
    Devices
    Firm
    Boston Scientific Corporation
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    December 30, 2020
    Initiation Date
    November 18, 2020
    Classification Date
    December 22, 2020
    Address
    1 Scimed Pl, N/A, Maple Grove, MN, 55311-1565, United States

    Description

    IceRod" 1.5 i-Thaw" Cryoablation Needle

    Reason

    Complaint trend regarding needle shaft gas leaks.

    Code Info

    UPN: FPRPR4009 UDIs: 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204, 7290104830204 Batch Numbers: U1362, U1217, U0957, U0283, U0282, U0087, T0819, T0392, A6883, A6657, A2043, A1954, A1669, A1532, A1501, A1476, A1329

    Distribution

    Nationwide

    Quantity

    262 units