CPAP, BiPAP, and Ventilator recall in Canada: foam degradation risk
In plain language
This recall involves Philips Respironics CPAP, BiPAP, and mechanical ventilators sold in Canada. They are being recalled because the sound abatement foam may degrade, and particles or chemicals could enter the device's air pathway. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model numbers listed in the official notice.
- Contact Philips Respironics for further instructions.
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Affected products
BIPAP AUTOSV WITH SMARTCARD INT
Model: 1044114
Lot: All lots
BIPAP AUTOSV WITH SMARTCARD INT, CORE PKG
Model: 1044235
Lot: All lots
BIPAP SYNCHRONY VENTILATORY SUPPORT SYSTEM WITH SMARTCARD
Model: 1029756 CA1029756
Lot: All lots
BIPAP SYNCHRONY VENTILATORY SUPPORT SYSTEM WITH SMARTCARD-CORE PACK
Model: CA1029759
Lot: All lots
TRILOGY 100 VENTILATOR, CANADA
Model: CA1054096 CA1054096B U1054260
Lot: All lots
TRILOGY 100 VENTILATOR-INTERNATIONAL
Model: 1054096 U1054096
Lot: All lots
BIPAP AVAPS CORE PACKAGE, NORTH AMERICA
Model: 1029750
Lot: All lots
BIPAP AUTOSV ADVANCED/ENCORE SMARTCARD
Model: 1044288
Lot: All lots
BIPAP AUTOSV ADVANCED/ENCORE SMARTCARD/HEATED HUMIDIFIER
Model: 1044289
Lot: All lots
TRILOGY 200, CANADA
Model: CA1032800 CA1032800B
Lot: All lots
BIPAP A30 SYSTEM-VENTILATOR
Model: 1076577 1111147
Lot: All lots
BIPAP A30 SYSTEM-VENTILATOR & SYSTEM ONE A-SERIES HEATED HUMIDIFIER
Model: 1076578 1111148
Lot: All lots
BIPAP A40, CANADA
Model: 1076579 1111173
Lot: All lots
BIPAP A40, CANADA, CORE PACKAGE
Model: 1111174
Lot: All lots
Why this matters
Inhalation hazard from foam particles or chemicals
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: 1029750, 1029756 CA1029756, 1044114, 1044235, 1044288, 1044289, 1054096 U1054096, 1076577 1111147, 1076578 1111148, 1076579 1111173, 1111174, CA1029759, CA1032800 CA1032800B, CA1054096 CA1054096B U1054260
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?
Inhalation hazard from foam particles or chemicals
What should consumers do?
Stop using the product immediately. Check the model numbers listed in the official notice. Contact Philips Respironics for further instructions.
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. Inhalation hazard from foam particles or chemicals
When was this product recalled?
This product was recalled on June 23, 2021.
Is the Philips Respironics brand affected by this recall?
Yes, Philips Respironics products are affected by this recall. This recall involves Philips Respironics CPAP, BiPAP, and mechanical ventilators sold in Canada. They are being recalled because the sound abatement foam may degrade, and particles or chemicals could enter the device's air pathway. Stop using the product and follow the return/repair steps in the official notice.