CyPass Micro-Stent recall in Canada: May cause cell loss
In plain language
This recall involves the CyPass Micro-Stent Model 241, a medical device. It's being recalled because it may cause significant endothelial cell loss in patients. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer for instructions.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
CyPass Micro-Stent
Model: 8065754010 CYP 241
Lot: More than 100 numbers, contact manufacturer
Why this matters
May cause endothelial cell loss
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 100 numbers, contact manufacturer
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 8065754010 CYP 241
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?
May cause endothelial cell loss
What should consumers do?
Stop using the product immediately. Contact the manufacturer for 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. May cause endothelial cell loss
When was this product recalled?
This product was recalled on September 7, 2018.
Is the CyPass brand affected by this recall?
Yes, CyPass products are affected by this recall. This recall involves the CyPass Micro-Stent Model 241, a medical device. It's being recalled because it may cause significant endothelial cell loss in patients. Stop using the product and follow the return/repair steps in the official notice.