Novum IQ LVP recall in Canada: Performance issue
In plain language
This recall involves the Novum IQ LVP medical device sold in Canada. It's being recalled because of a potential for underinfusion if the "standby mode" feature is used, or if the device is powered off with the set loaded for an extended period. Contact the manufacturer for more information.
What to do
- ["Contact the manufacturer if you require additional information."]
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Novum IQ LVP
Model: 40700BAX
Lot: All lots.
Why this matters
Performance issue leading to underinfusion
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: All lots.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 40700BAX
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Performance issue leading to underinfusion
What should consumers do?
["Contact the manufacturer if you require additional information."]
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Performance issue leading to underinfusion
When was this product recalled?
This product was recalled on May 14, 2025.
Is the Baxter Healthcare Corporation brand affected by this recall?
Yes, Baxter Healthcare Corporation products are affected by this recall. This recall involves the Novum IQ LVP medical device sold in Canada. It's being recalled because of a potential for underinfusion if the "standby mode" feature is used, or if the device is powered off with the set loaded for an extended period. Contact the manufacturer for more information.