Respironics Omnilab Advanced and BiPAP A40 recall in Canada: Device failure risk
In plain language
This recall involves Respironics Omnilab Advanced and BiPAP A40 devices sold in Canada. They are being recalled because a plastic component in the motor may degrade, which could cause the device to fail suddenly during use. Stop using the product and contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact the manufacturer for additional information.
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Affected products
Omnilab Advanced, Domestic Core
Model: 1111124
Lot: L28664722DB58, L28664717A69D
Bipap A40, Canada, Core Package
Model: 1111174
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Device failure risk
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: L28664722DB58, L28664717A69D, More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 1111124, 1111174
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?
Device failure risk
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. Device failure risk
When was this product recalled?
This product was recalled on August 31, 2022.
Is the Respironics Inc. brand affected by this recall?
Yes, Respironics Inc. products are affected by this recall. This recall involves Respironics Omnilab Advanced and BiPAP A40 devices sold in Canada. They are being recalled because a plastic component in the motor may degrade, which could cause the device to fail suddenly during use. Stop using the product and contact the manufacturer for more information.