Balloon Guide Catheter recall in Canada: incorrect product packaging
In plain language
This recall involves the Balloon Guide Catheter sold in Canada. It's being recalled because some packaging contains an incorrect product. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check model and lot numbers.
- Contact Stryker Neurovascular for return instructions.
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Affected products
Balloon Guide Catheter
Model: 90074
Lot: 0000010779
Why this matters
Incorrect product packaging
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: 0000010779
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 90074
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?
Incorrect product packaging
What should consumers do?
Stop using the product immediately. Check model and lot numbers. Contact Stryker Neurovascular for return 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. Incorrect product packaging
When was this product recalled?
This product was recalled on January 9, 2019.