IntelePACS recall in Canada: Incorrect diagnosis risk
In plain language
This recall involves IntelePACS (Image Fusion Module) software sold in Canada. It's being recalled because an incorrect calculation could lead to a wrong diagnosis. This issue happens on days with a daylight savings time change. This recall is for healthcare professionals.
What to do
- Contact the manufacturer for more information.
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Affected products
IntelePACS (Image Fusion Module)
Model: INTELEPACS
Why this matters
Incorrect diagnosis risk
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 model number
Model numbers are typically on the product label or packaging.
Affected models: INTELEPACS
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?
Incorrect diagnosis risk
What should consumers do?
Contact the manufacturer for more 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. Incorrect diagnosis risk
When was this product recalled?
This product was recalled on February 19, 2025.
Is the INTELERAD MEDICAL SYSTEMS INCORPORATED brand affected by this recall?
Yes, INTELERAD MEDICAL SYSTEMS INCORPORATED products are affected by this recall. This recall involves IntelePACS (Image Fusion Module) software sold in Canada. It's being recalled because an incorrect calculation could lead to a wrong diagnosis. This issue happens on days with a daylight savings time change. This recall is for healthcare professionals.