BEUDAMED
    FDA Recall Open, Classified

    RAPTAR Laser Range Finders

    Recall: Z-0001-2022 · Initiated April 21, 2021

    Recall

    Recall Number
    Z-0001-2022
    Event Number
    88735
    Firm
    Potomac River Group, Corp.
    FEI Number
    3004918946
    Product Code
    REP
    Status
    Open, Classified
    Root Cause
    Radiation Control for Health and Safety Act
    Initiated
    April 21, 2021
    Address
    19775 Belmont Executive Plz, Ashburn, VA, 20147-7600

    Description

    RAPTAR Laser Range Finders

    Reason

    RAPTAR units are capable of being field modified to enable the use of the higher power visible and IR laser pointers and the IR Illuminator.

    Action

    Potomac River Group (PRG) sent communications to the purchasers of the affected units that were locked in the eye safe mode and distributed without the keys. PRG expects to offer all affected purchasers at least a refund option. PRG s ability to offer a repair option is contingent upon assistance from Wilcox, which is the only entity PRG is aware of that has the ability to render the units compliant with FDA specifications.

    Distribution

    US Nationwide

    Quantity

    62 units