Novum Iq Large Volume Pump Unapproved Adhesive
Brand(s)
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
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