F&P SleepStyle CPAP Device recall in Canada: firmware anomaly
In plain language
This recall involves the F&P SleepStyle CPAP Device sold in Canada. It's being recalled because a firmware issue may prevent the device from recording clinical data and could delay remote prescription changes. 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 more information on affected serial numbers.
- Follow the instructions from the manufacturer regarding the firmware anomaly.
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Affected products
F&P SleepStyle CPAP Device
Model: SPSAAN
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Firmware anomaly affecting data recording
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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: SPSAAN
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?
Firmware anomaly affecting data recording
What should consumers do?
Stop using the product immediately. Contact the manufacturer for more information on affected serial numbers. Follow the instructions from the manufacturer regarding the firmware anomaly.
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. Firmware anomaly affecting data recording
When was this product recalled?
This product was recalled on April 3, 2018.
Is the F&P SleepStyle brand affected by this recall?
Yes, F&P SleepStyle products are affected by this recall. This recall involves the F&P SleepStyle CPAP Device sold in Canada. It's being recalled because a firmware issue may prevent the device from recording clinical data and could delay remote prescription changes. Stop using the product and follow the return/repair steps in the official notice.