Health product recall

Novum Iq Large Volume Pump Unapproved Adhesive

Last updated

Summary

Product
Novum Iq Large Volume Pump Unapproved Adhesive
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalogue number
Novum Iq Large Volume Pump More than 10 numbers, contact manufacturer. 40700BAX

Issue

Baxter Corporation is issuing an urgent medical device correction for specific Novum Iq LVPs where an unapproved adhesive was used in error during service for the re-installation of the slide clamp assemblies, which can result in in the slide clamp not ejecting properly or the door not opening.

Recall start date: October 26, 2023

Additional information

Previous recalls or alerts
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
Baxter Healthcare Corporation
1 Baxter Parkway, Deerfield, Illinois, United States, 60015
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74563