Tempus Pro Monitor recall in Canada: performance issues
In plain language
This recall involves the Tempus Pro Monitor, a medical device used in healthcare settings in Canada. It's being recalled because the device may fail to start normally, freeze, or reboot, and could also produce inaccurate ECG measurements. Healthcare professionals should contact the manufacturer for additional information.
What to do
- Contact the manufacturer for additional information.
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Affected products
Tempus Pro Monitor
Model: 00-1007-R, 00-1024-R, 00-1026-R
Lot: Not applicable
Why this matters
Performance issues leading to device inoperability or inaccurate measurements
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: Not applicable
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 00-1007-R, 00-1024-R, 00-1026-R
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 issues leading to device inoperability or inaccurate measurements
What should consumers do?
Contact the manufacturer for 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 issues leading to device inoperability or inaccurate measurements
When was this product recalled?
This product was recalled on April 25, 2025.
Is the Remote Diagnostic Technologies Limited brand affected by this recall?
Yes, Remote Diagnostic Technologies Limited products are affected by this recall. This recall involves the Tempus Pro Monitor, a medical device used in healthcare settings in Canada. It's being recalled because the device may fail to start normally, freeze, or reboot, and could also produce inaccurate ECG measurements. Healthcare professionals should contact the manufacturer for additional information.