Events

Recall of ANCHOR GUIDE HOLDER - LORAD

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BARD 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
    25744
  • Event Risk Class
    III
  • Event Initiated Date
    2016-08-25
  • 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
    Bard is notifying customers that specific lots of encor needle guide insert 10g may instead contain a smaller diameter (12g) insert. the 12g needle guide insert does not allow the larger 10g needle probe to pass through rendering the device unusable.

Device

ANCHOR GUIDE HOLDER - LORAD
  • Model / Serial
    Model Catalog: ENCFINSERT10G (Lot serial: >10 NUMBERS CONTACT MFR)
  • Product Description
    ENCOR NEEDLE GUIDE INSERT 10G
  • Manufacturer
    BARD CANADA INC.

Manufacturer

BARD CANADA INC.