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Tempus pro
Official notice
9 Dec 2025
Last checked
9 Dec 2025
An official Health Canada notice concerns Tempus pro. The user/operator manual references the term 'invasive pressure', which includes intracranial pressure (ICP) and bladder pressure (BDR) as selectable channel labels. However, these measurements on the Tempus Pro monitor have not been tested or validated for accuracy. The device is only cleared for invasive blood pressure (IBP) measurements. Published 2025-12-09.
What to do now
Contact the manufacturer if you require additional information.
Recall number
81341
Official notice
2025-12-09
The hazard
The hazard
The user/operator manual references the term 'invasive pressure', which includes intracranial pressure (ICP) and bladder pressure (BDR) as selectable channel labels. However, these measurements on the Tempus Pro monitor have not been tested or validated for accuracy. The device is only cleared for invasive blood pressure (IBP) measurements.
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
Product 1
Product 2
Product 3
Product 4
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
Brand: Remote Diagnostic, Tempus Pro.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
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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