Official recall record
Novum Iq Large Volume Pump Unapproved Adhesive
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2023-11-08
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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