Tri-Staple™ 2.0 Black Intelligent Reload recall in Canada: performance issue
In plain language
This recall involves the Tri-Staple™ 2.0 Black Intelligent Reload, a medical device. It's being recalled because a component may break, leading to a misfire during surgery. This could result in serious injury or death. This recall is primarily for healthcare professionals.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Tri-Staple™ 2.0 Black Intelligent Reload
Model: SIG60AXT
Lot: N2D0195Y
Why this matters
Serious injury or death due to 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: N2D0195Y
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: SIG60AXT
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?
Serious injury or death due to device malfunction
What should consumers do?
Contact the manufacturer if you require 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. Serious injury or death due to device malfunction
When was this product recalled?
This product was recalled on February 8, 2023.
Is the COVIDIEN LLC brand affected by this recall?
Yes, COVIDIEN LLC products are affected by this recall. This recall involves the Tri-Staple™ 2.0 Black Intelligent Reload, a medical device. It's being recalled because a component may break, leading to a misfire during surgery. This could result in serious injury or death. This recall is primarily for healthcare professionals.