Events

Recall of SHERIDAN PREFORMED UNCUFFED TRACHEAL TUBES NASAL WITH TWO MURPHY EYES

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by TRUDELL MEDICAL MARKETING LIMITED.

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
    42021
  • Event Risk Class
    II
  • Event Initiated Date
    2015-01-13
  • 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
    Teleflex medical is recalling the hudson rci/performed uncuffed tracheal tube nasal due to incorrect product labeling. the affected product packaging is incorrectly labeled as being a "cuffed oral et tube." the correct product labeling is "uncuffed nasal et tube.".

Device

SHERIDAN PREFORMED UNCUFFED TRACHEAL TUBES NASAL WITH TWO MURPHY EYES
  • Model / Serial
    Model Catalog: 5-22110 (Lot serial: 01M1300076)
  • Product Description
    Hudson RCI Sheridan/Performed Uncuffed Tracheal Tube Nasal
  • Manufacturer
    TRUDELL MEDICAL MARKETING LIMITED

Manufacturer

TRUDELL MEDICAL MARKETING LIMITED