BEUDAMED
    FDA Recall Terminated

    Model LightLas 532 Opthalmic Photocoagulator Laser

    Recall: Z-0228-04 · Initiated November 11, 2003

    Recall

    Recall Number
    Z-0228-04
    Event Number
    27819
    Firm
    LightMed USA Inc
    FEI Number
    3003976404
    Product Code
    HQF
    Status
    Terminated
    Root Cause
    Other
    Initiated
    November 11, 2003
    Posted
    December 17, 2003
    Terminated
    December 16, 2003
    Address
    1030 Calle Cordillera, Ste 101, San Clemente, CA, 92673-6234

    Description

    Model LightLas 532 Opthalmic Photocoagulator Laser

    Reason

    Firm needed to include calibration procedures in user guide.

    Action

    Firm fedexed new user manuals with calibration procedures to each consignee on 11/11/2003.

    Distribution

    CA, GA

    Quantity

    2