Recall of Alcon LuxOR LX3 Microscope Floor Stand(used with LuxOR LX3 and Q-VUE LX3 Ophthalmic Microscopes 175mm and 200mm)

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Alcon Laboratories Australia Pty Ltd.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    RC-2017-RN-00727-1
  • Event Risk Class
    Class II
  • Event Initiated Date
    2017-06-02
  • Event Country
  • Event Source
    DHTGA
  • Event Source URL
  • Notes / Alerts
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Australia.
  • Extra notes in the data
  • Reason
    Alcon has observed that multiple shipments or forceful impact to a caster on a luxor lx3 microscope may stress the microscope base, which could contribute to a caster breaking or detaching from the base. during an in-facility transfer, should a caster break or detach from the base while the microscope arm is not in the most inward locked position, the unit may tip if the microscope arm is extended over the location of the broken caster. this may lead to the potential for physical injury from the microscope tipping or falling.To date, two incidents of physical injury have been reported overseas in conjunction with this issue.
  • Action
    Alcon will contact users to schedule an appointment to inspect and retrofit LuxOR LX3 units with new bases and/or an updated caster configuration. In the interim, users are advised to ensure the articulating microscope arm is placed in a stowed and locked position over the microscope base and protect the casters from forceful impact. (Refer to recall notification for further details). Users are to contact their Alcon technical representative if they need to transport their unit to an off-site location or have immediate concerns about their unit.

Device

  • Model / Serial
    Alcon LuxOR LX3 Microscope Floor Stand(used with LuxOR LX3 and Q-VUE LX3 Ophthalmic Microscopes 175mm and 200mm)Catalogue Number: 8065752560ARTG Number: 210550
  • Manufacturer

Manufacturer