Tempus Pro recall in Canada: Medical device performance issue
In plain language
This recall involves the Tempus Pro medical device sold in Canada. It's being recalled because an error may occur during or after video laryngoscope use, which can prevent viewing of patient vital signs. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer for additional information.
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Affected products
Tempus Pro - 92512
Model: 00-1007-R
Lot: Not applicable.
Why this matters
Medical device performance issue
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
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?
Medical device performance issue
What should consumers do?
Stop using the product immediately. 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. Medical device performance issue
When was this product recalled?
This product was recalled on September 1, 2023.
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 medical device sold in Canada. It's being recalled because an error may occur during or after video laryngoscope use, which can prevent viewing of patient vital signs. Stop using the product and follow the return/repair steps in the official notice.