Events

Recall of TEXIUM CLOSED MALE LUER WITH FEMALE CAP

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

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
    13171
  • Event Risk Class
    II
  • Event Initiated Date
    2007-10-11
  • 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
    6 complaints have been received where there have been leaks at the female end of the texium device when connected to the male spin luer at the end of a primary set. no complaints have occurred in canada.

Device

TEXIUM CLOSED MALE LUER WITH FEMALE CAP
  • Model / Serial
    Model Catalog: 10012241 (Lot serial: ALL LOTS)
  • Product Description
    TEXIUM CLOSED MALE LUER
  • Manufacturer
    CARDINAL HEALTH CANADA

Manufacturer

CARDINAL HEALTH CANADA
  • Manufacturer Address
    VAUGHAN
  • Manufacturer Parent Company (2017)
    Cardinal Health
  • Source
    HC