Events

Recall of Coiled Tube Baxter Infusors (Portable Elastomeric Infusion Systems)

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Baxter Healthcare Pty Ltd.

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-2013-RN-00568-1
  • Event Risk Class
    Class I
  • Event Initiated Date
    2013-06-06
  • Event Country
    Australia
  • Event Source
    DHTGA
  • Event Source URL
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2013-RN-00568-1
  • 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
    There has been an increase in complaints of leaks at the distal male luer and luer cap.
  • Action
    End users and distributors are requested to locate and remove all affected units from use. The affected product should be returned to Baxter for a credit.

Device

Coiled Tube Baxter Infusors (Portable Elastomeric Infusion Systems)

Manufacturer

Baxter Healthcare Pty Ltd