StealthStation S8 software recall in Canada: Performance issues
In plain language
This recall involves the StealthStation S8 software application sold in Canada. It's being recalled because of two software anomalies that can affect performance during spine procedures. Stop using the product and contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact Medtronic Navigation, Inc. for additional information.
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Affected products
StealthStation S8 software application
Model: 9735762
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Performance issues
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: 9735762
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?
Performance issues
What should consumers do?
Stop using the product immediately. Contact Medtronic Navigation, Inc. for additional information.
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. Performance issues
When was this product recalled?
This product was recalled on September 4, 2024.
Is the Medtronic Navigation, Inc brand affected by this recall?
Yes, Medtronic Navigation, Inc products are affected by this recall. This recall involves the StealthStation S8 software application sold in Canada. It's being recalled because of two software anomalies that can affect performance during spine procedures. Stop using the product and contact the manufacturer for more information.