Recall of LTV SERIES VENTILATOR

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by PULMONETIC SYSTEMS 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
    14841
  • Event Risk Class
    II
  • Event Initiated Date
    2003-01-20
  • 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
    Printed circuit board malfunction may result in ventilator becoming non-functional with an unlikely possibility of no audible alarm sounding to alert caregiver.

Device

  • Model / Serial
    Model Catalog: 10784 (Lot serial: ); Model Catalog: LTV 900 (Lot serial: ); Model Catalog: LTV 800 (Lot serial: ); Model Catalog: LTV 950 (Lot serial: )
  • Product Description
    LTV 900 950 and 1000 series
  • Manufacturer

Manufacturer

  • Manufacturer Address
    MINNEAPOLIS
  • Source
    HC