Xper Flex Cardio Physiomonitoring System recall in Canada: inaccurate readings
In plain language
This recall involves the Xper Flex Cardio Physiomonitoring System-Main Unit (FC2010) sold in Canada. It's being recalled because the real-time numeric value for ventricular end-diastolic pressure (EDP) displayed on the Live Display may be inaccurate. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model number FC2010.
- Contact Philips for more information.
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Affected products
Xper Flex Cardio Physiomonitoring System-Main Unit
Model: FC2010
Lot: All lots
Why this matters
Inaccurate medical readings
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: FC2010
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?
Inaccurate medical readings
What should consumers do?
Stop using the product immediately. Check the model number FC2010. Contact Philips 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. Inaccurate medical readings
When was this product recalled?
This product was recalled on April 13, 2018.
Is the Philips brand affected by this recall?
Yes, Philips products are affected by this recall. This recall involves the Xper Flex Cardio Physiomonitoring System-Main Unit (FC2010) sold in Canada. It's being recalled because the real-time numeric value for ventricular end-diastolic pressure (EDP) displayed on the Live Display may be inaccurate. Stop using the product and follow the return steps in the official notice.