Microstream™ Advance Intubated CO2 Filter Line, VitaLine® Intubated CO2 FilterLine and FilterLine® Intubated CO2 Filter Line
In plain language
This recall involves Microstream™ Advance Intubated CO2 Filter Line, VitaLine® Intubated CO2 FilterLine, and FilterLine® Intubated CO2 Filter Line products sold in Canada. They are being recalled due to performance issues related to disconnecting an adapter from a patient's endotracheal tube. Healthcare professionals should contact the manufacturer for updated instructions.
What to do
- Contact the manufacturer, Philips Medical Systems, for additional information.
- Review the updated instructions for use (IFU) addendum.
- Follow instructions for safe use of the airway adapter.
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Affected products
Filterline Set H Infant/Neonatal
Model: M1923A
Lot: Not applicable.
Filterline Set Adult/Pediatric
Model: M1920A
Lot: Not applicable.
Filterline Set H Adult/Pediatric
Model: M1921A
Lot: Not applicable.
Why this matters
Performance issues
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: Not applicable.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: M1920A, M1921A, M1923A
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?
Performance issues
What should consumers do?
Contact the manufacturer, Philips Medical Systems, for additional information. Review the updated instructions for use (IFU) addendum. Follow instructions for safe use of the airway adapter.
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. Performance issues
When was this product recalled?
This product was recalled on April 29, 2025.
Is the PHILIPS MEDICAL SYSTEMS brand affected by this recall?
Yes, PHILIPS MEDICAL SYSTEMS products are affected by this recall. This recall involves Microstream™ Advance Intubated CO2 Filter Line, VitaLine® Intubated CO2 FilterLine, and FilterLine® Intubated CO2 Filter Line products sold in Canada. They are being recalled due to performance issues related to disconnecting an adapter from a patient's endotracheal tube. Healthcare professionals should contact the manufacturer for updated instructions.