Recall of INFUSOR

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
    95711
  • Event Risk Class
    II
  • Event Initiated Date
    2014-04-14
  • 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
    Baxter corporation is issuing a safety alert for coiled tube infusors noting that a labeling error previously communicated to customers on march 5 2014 when combined with all other use factors can contribute to infusion rates in excess of 30% greater than the nominal (labeled) flow rate. delivery of medication at an infusion rate faster than intended may lead to toxicity and changes to efficacy that require medical intervention.

Device

  • Model / Serial
    Model Catalog: 2C1073KJP (Lot serial: >100 NUMBERS CONTACT MFR); Model Catalog: 2C1075KJP (Lot serial: >100 NUMBERS CONTACT MFR); Model Catalog: 2C1080KJP (Lot serial: >100 NUMBERS CONTACT MFR); Model Catalog: 2C1071KJP (Lot serial: >100 NUMBERS CONTACT MFR); Model Catalog: 2C1082KJP (Lot serial: >100 NUMBERS CONTACT MFR)
  • Product Description
    COILED TUBE INFUSOR
  • Manufacturer

Manufacturer