Events

Recall of (1) Light system SA (2) enLIGHTen Enrighton

According to Pharmaceuticals and Medical Devices Agency, Japan, this recall involved a device in Japan that was produced by Cutera Corporation.

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
    2-8029
  • Date
    2018-02-01
  • Event Country
    Japan
  • Event Source
    PMDAJ
  • Event Source URL
    http://www.info.pmda.go.jp/rgo/MainServlet?recallno=2-8029
  • Notes / Alerts
    Japanese data is current through August 2018. All of the data comes from the Japanese Pharmaceuticals and Medical Devices Agency, 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 Japan.
  • Extra notes in the data
    Recovery end

Device

(1) Light system SA (2) enLIGHTen Enrighton
  • Model / Serial
  • Product Description
    (1) Xenon light ray therapy equipment (2) Neodymium · Yag Laser
  • Manufacturer
    Cutera Corporation

Manufacturer

Cutera Corporation