T2 Tibial Nail System recall in Canada: Medical device defect
In plain language
This recall involves the T2 Tibial Nail System - Nail Insertion Sleeve Elastic sold in Canada. It's being recalled because the inner diameter of some sleeves does not match the label. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model and lot numbers.
- Contact Stryker Trauma GmbH for further instructions.
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Affected products
T2 TIBIAL NAIL SYSTEM- NAIL INSERTION SLEEVE ELASTIC
Model: 1806-1406S, 1806-1407S
Lot: K03CC4F, K03CC50
Why this matters
Medical device defect
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: K03CC4F, K03CC50
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 1806-1406S, 1806-1407S
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?
Medical device defect
What should consumers do?
Stop using the product immediately. Check model and lot numbers. Contact Stryker Trauma GmbH for further 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. Medical device defect
When was this product recalled?
This product was recalled on May 26, 2021.