Events

Recall of ECLIPSE OXYGEN SYSTEM

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by CHART SEQUAL TECHNOLOGIES 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
    130223
  • Event Risk Class
    I
  • Event Initiated Date
    2010-01-20
  • 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
    Eclipse oxygen system units may experience premature wear on electrical connector between battery bridge printed circuit board and power manager printed circuit board that could lead to temporary power interruption when operating from power cartridge causing unit to sound an alarm and shut down.

Device

ECLIPSE OXYGEN SYSTEM
  • Model / Serial
    Model Catalog: (Lot serial: 063005184); Model Catalog: (Lot serial: 073006282); Model Catalog: (Lot serial: 073000585 073007840); Model Catalog: (Lot serial: 073006062 073002301); Model Catalog: (Lot serial: 073004651073003155073004456); Model Catalog: (Lot serial: 073002972)
  • Product Classification
    Anesthesiology Devices
  • Product Description
    SEQUAL ECLIPSE OXYGEN SYSTEM
  • Manufacturer
    CHART SEQUAL TECHNOLOGIES INC.

Manufacturer

CHART SEQUAL TECHNOLOGIES INC.