Events

Recall of ISOLINE 2CR DEFIBRILLATION LEAD

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

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
    50961
  • Event Risk Class
    II
  • Event Initiated Date
    2011-10-20
  • 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
    A batch of isoline defibrillation leads was labelled with an incorrect use before date (ubd) which was greater than the maximum of 36 months shelf life. the date printed on the labels was 5 may 2013 while the correct ubd is 21 september 2012.

Device

ISOLINE 2CR DEFIBRILLATION LEAD
  • Model / Serial
    Model Catalog: 2CR-6 (Lot serial: S2CR605347); Model Catalog: 2CR-6 (Lot serial: S2CR605346)
  • Product Description
    ISOLINE 2CR6 DEFIBRILLATION LEADS
  • Manufacturer
    LIVANOVA CANADA CORP.

Manufacturer

LIVANOVA CANADA CORP.
  • Manufacturer Address
    MARKHAM
  • Manufacturer Parent Company (2017)
    LivaNova PLC
  • Source
    HC