Events

Recall of ENDODONTIC REDUCER CONTRA ANGLE 18:1 HANDPIECE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by HENRY SCHEIN CANADA INC..

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
    23170
  • Event Risk Class
    III
  • Event Initiated Date
    2011-09-13
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Extra notes in the data
  • Reason
    It was discovered that the endodotic reducer contra angle 18:1 handpiece was not licensed for sale in canada.

Device

ENDODONTIC REDUCER CONTRA ANGLE 18:1 HANDPIECE
  • Model / Serial
    Model Catalog: 815-9010 (Lot serial: all lots); Model Catalog: 815-9008 (Lot serial: all lots)
  • Product Description
    ENDODONTIC REDUCER CONTRA ANGLE 18:1 HANDPIECE
  • Manufacturer
    HENRY SCHEIN CANADA INC.

Manufacturer

HENRY SCHEIN CANADA INC.
  • Manufacturer Address
    NIAGARA-ON-THE-LAKE
  • Manufacturer Parent Company (2017)
    Henry Schein Inc
  • Source
    HC