Recall of Inhalo Medical Oxygen with Integrated Pressure Regulator/FlowmeterBOC

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by BOC 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
    RC-2017-RN-00215-1
  • Event Risk Class
    Class II
  • Event Initiated Date
    2017-02-13
  • Event Country
  • Event Source
    DHTGA
  • Event Source URL
  • Notes / Alerts
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 Australia.
  • Extra notes in the data
  • Reason
    The pressure gauges supplied to boc as part of the inhalo device, may in rare circumstances, have a broken pointer. this failure mode may result in the gauge pointer moving independently of actual cylinder pressure. this will result in inaccurate pressure readings being observed. the situation has been observed where, with a cylinder in a vertical position, the pressure gauge pointer can indicate the cylinder is full, when in fact there is reduced content within the cylinder.
  • Action
    Customers are advised to confirm that the stock they are using is not faulty and has sufficient contents to administer therapy i.e., all 400CD Inhalo cylinders will need to be checked prior to use as per the Pressure Gauge Check work instruction provided with the customer letter. If no fault is identified, customers can continue to use the product, there is no need to contact BOC. If a faulty pressure gauge is identified, please contact BOC immediately for a free of charge replacement. BOC has implemented additional product testing prior to release from their filling sites, however there is a remote possibility that a pressure gauge pointer may fail during transit/handling.

Device

  • Model / Serial
    Inhalo Medical Oxygen with Integrated Pressure Regulator/FlowmeterBOC Product Code: 400CDARTG Number: 187646
  • Manufacturer

Manufacturer