Omnilab Advanced recall in Canada: ventilator performance issues
In plain language
This recall involves Omnilab Advanced Domestic and Omnilab Advanced Domestic Core devices sold in Canada. They are being recalled because a ventilator inoperative alarm may lead to interruption or loss of therapy. 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: 1111123, 1111124
Lot: All lots
Omnilab Advanced, Domestic
Model: 1111122
Lot: All lots
Why this matters
Interruption or loss of therapy, potentially leading to serious health issues or death
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: 1111122, 1111123, 1111124
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?
Interruption or loss of therapy, potentially leading to serious health issues or death
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. Interruption or loss of therapy, potentially leading to serious health issues or death
When was this product recalled?
This product was recalled on May 15, 2024.
Is the Respironics Inc. brand affected by this recall?
Yes, Respironics Inc. products are affected by this recall. This recall involves Omnilab Advanced Domestic and Omnilab Advanced Domestic Core devices sold in Canada. They are being recalled because a ventilator inoperative alarm may lead to interruption or loss of therapy. Stop using the product and contact the manufacturer for more information.