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Novum iq large volume pump unapproved adhesive
Official notice
8 Nov 2023
Last checked
8 Nov 2023
An official Health Canada notice concerns Novum iq large volume pump unapproved adhesive. 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 Published 2023-11-08.
What to do now
Contact the manufacturer if you require additional information.
Recall number
74563
Official notice
2023-11-08
The hazard
The hazard
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
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Affected products
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Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Manufacturer
Phone
Brand: Baxter Healthcare, Novum Iq Large Volume Pump Unapproved Adhesive.
Source & status
Source & status
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Tier
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Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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