Recall of PENTAX DUODENOSCOPE

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

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
    29564
  • Event Risk Class
    II
  • Event Initiated Date
    2016-03-02
  • Event Country
  • 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
    Pentax medical has been working with the u.S. food and drug administration ("fda") as part of an industry-wide initiative to determine what additional steps if any could be undertaken to reduce the risk of infection in flexible endoscopes used for ercp procedures. the updated reprocessing ifus were developed after rigorous validation testing and ongoing discussions with fda to further enhance the safety margin and show with a high degree of assurance that the updated reprocessing ifus when followed correctly effectively clean and disinfect the duodenoscope.

Device

  • Model / Serial
    Model Catalog: ED-3490TK (Lot serial: >10 NUMBERS CONTACT MFG)
  • Product Description
    PENTAX VIDEO DUODENOSCOPE
  • Manufacturer

Manufacturer

  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
  • Source
    HC