Events

Recall of ECC.O INTEGRATED MINI-BYPASS SYSTEM WITH PRECONNECTED TUBINGS

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
    36127
  • Event Risk Class
    II
  • Event Initiated Date
    2008-12-31
  • 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
    Sorin group italia received reports of restricted or blocked flow at the outlet of the mini-bypass bag adopted into perfusion tubing sets designed for mini-bypass systems for the models and lots specified.

Device

ECC.O INTEGRATED MINI-BYPASS SYSTEM WITH PRECONNECTED TUBINGS
  • Model / Serial
    Model Catalog: 085339 (Lot serial: > 10 NUMBERS CONTACT MFR); Model Catalog: 084221 (Lot serial: > 10 NUMBERS CONTACT MFR)
  • Product Description
    ECC.O INTEGRATED MINI-BYPASS SYSTEM
  • Manufacturer
    LIVANOVA CANADA CORP.

Manufacturer

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