Events

Recall of JARIT MONOPOLAR CABLE

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

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
    22531
  • Event Risk Class
    III
  • Event Initiated Date
    2013-02-12
  • 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
    Distribution of addendum to ifu emphasizing wanrnings and precautions already contained in the ifu and additional precautions applicable to the use of electrosurgical equipment in a health care facility environment.

Device

JARIT MONOPOLAR CABLE
  • Model / Serial
    Model Catalog: 600-290 (Lot serial: ALL LOTS)
  • Product Description
    Integra Jarit Monopolar Cable
  • Manufacturer
    INTEGRA CANADA ULC.

Manufacturer

INTEGRA CANADA ULC.