Filter/HME Twinstar Plus recall in Canada: labelling and packaging issue
In plain language
This recall involves Filter/HME Twinstar Plus medical devices sold in Canada. It's being recalled because of issues with labelling and packaging that could lead to increased breathing resistance. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
- Monitor airway pressure and volume if using the device.
- Change the filter if resistance increases.
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Affected products
Filter/HME Twinstar Plus
Model: MP05800, MP05805, MP05810, MP05815, MP05820
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Increased inspiratory resistance
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: MP05800, MP05805, MP05810, MP05815, MP05820
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?
Increased inspiratory resistance
What should consumers do?
Contact the manufacturer if you require additional information. Monitor airway pressure and volume if using the device. Change the filter if resistance increases.
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. Increased inspiratory resistance
When was this product recalled?
This product was recalled on August 4, 2023.
Is the Draegerwerk Ag & Co. Kgaa brand affected by this recall?
Yes, Draegerwerk Ag & Co. Kgaa products are affected by this recall. This recall involves Filter/HME Twinstar Plus medical devices sold in Canada. It's being recalled because of issues with labelling and packaging that could lead to increased breathing resistance. Healthcare professionals should contact the manufacturer for more information.