Events

Recall of DUAL LUER LOCK CAP MALE/FEMALE PORT PROTECTOR

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

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
    43276
  • Event Risk Class
    I
  • Event Initiated Date
    2013-09-17
  • 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
    Baxter is initiating a recall for lot 10043 for product code 2c6250 due to loose particulate matter found in the packaging. particulate matter entering the fluid path from the luer lock caps may result in embolic events.

Device

DUAL LUER LOCK CAP MALE/FEMALE PORT PROTECTOR

Manufacturer

BAXTER CORPORATION