BEUDAMED
    FDA Enforcement Class II Ongoing

    Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 30cm, Material CA30L1

    Recall: Z-0560-2018 · Reported February 14, 2018

    Enforcement

    Recall Number
    Z-0560-2018
    Event ID
    79075
    Classification
    Class II
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Covidien LLC
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    February 14, 2018
    Initiation Date
    August 7, 2017
    Classification Date
    February 8, 2018
    Address
    60 Middletown Ave, N/A, North Haven, CT, 06473-3908, United States

    Description

    Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 30cm, Material CA30L1

    Reason

    The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.

    Code Info

    UDI 10884521189553, Lot codes: S5LG004PX,S6AG001X,S6BG002X,S6BG005X,S6BG016PX,S6CG003X,S6CG005X,S6CG017X,S6DG004X,S6EG001X,S6FG001X,S6FG006X,S6FG010X,S6KG002X,S6KG006PRX,S6KG006PX,S6LG004X,S6MG002X,S7CG001PCX,S7CG011PCX,S7CG015CX,S7EG001X,S7EG003X,S7FG011PX

    Distribution

    Nationwide including PR, Canada, China

    Quantity

    N/A