Events

Safety Alert for LA 5 Burs

According to Department of Health, this safety alert involved a device in Hong Kong that was produced by Beavers Dental.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Safety alert
  • Date
    2011-12-02
  • Event Country
    Hong Kong
  • Event Source
    DH
  • Event Source URL
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20111202a.html
  • Notes / Alerts
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • Extra notes in the data
    Medical Device Safety Alert
  • Reason
    Field safety notice: beavers dental la 5 burs beavers dental is conducting a recall on la 5 burs. the manufacturer found that one lot of la5 burs actually contained fg 557 burs. according to the manufacturer, there are no hong kong consignees affected by this recall. if you are in possession of the affected product, please contact your supplier for necessary actions.

Device

LA 5 Burs
  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Beavers Dental LA 5 Burs
  • Manufacturer
    Beavers Dental

Manufacturer

Beavers Dental