VentStar (N) 180 recall in Canada: Detached Y-piece
In plain language
This recall involves VentStar Anesthesia (N) 180 and VentStar Basic (N) 180 breathing circuits sold in Canada. They are being recalled because the Y-piece may detach from the ventilation hose due to a manufacturing error. This could cause a leak and hinder patient ventilation. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer for more information on affected lot numbers.
- Follow the manufacturer's instructions for return or replacement.
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Affected products
VentStar Anesthesia (N) 180
Model: MP00333
Lot: More than 10 numbers, contact manufacturer.
VentStar Basic (N) 180
Model: MP00353
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Hinder ventilation of the patient
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: MP00333, MP00353
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?
Hinder ventilation of the patient
What should consumers do?
Stop using the product immediately. Contact the manufacturer for more information on affected lot numbers. Follow the manufacturer's instructions for return or replacement.
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. Hinder ventilation of the patient
When was this product recalled?
This product was recalled on January 26, 2021.
Is the VentStar brand affected by this recall?
Yes, VentStar products are affected by this recall. This recall involves VentStar Anesthesia (N) 180 and VentStar Basic (N) 180 breathing circuits sold in Canada. They are being recalled because the Y-piece may detach from the ventilation hose due to a manufacturing error. This could cause a leak and hinder patient ventilation. Stop using the product and follow the return steps in the official notice.