Reprocessed LASSO 2515 NAV eco Variable Catheter recall in Canada: chip error
In plain language
This recall involves the Reprocessed LASSO 2515 NAV eco Variable Catheter sold in Canada. It's being recalled because an EEPROM chip error code may occur when used with CARTO EP Navigation Systems. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Contact Stryker Sustainability Solutions for more information.
- Follow the return instructions provided by the manufacturer.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Reprocessed LASSO 2515 NAV eco Variable Catheter
Model: D134301
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Device malfunction
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: D134301
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?
Device malfunction
What should consumers do?
Stop using the product immediately. Contact Stryker Sustainability Solutions for more information. Follow the return instructions provided by the manufacturer.
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. Device malfunction
When was this product recalled?
This product was recalled on January 29, 2018.