5.5 MM Arthrogarde Hip Access Cannula recall in Canada: manufacturing error
In plain language
This recall involves the 5.5 MM Arthrogarde Hip Access Cannula sold in Canada. It's being recalled due to a manufacturing error with the "J-Lock" feature. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model and lot numbers.
- Contact Smith & Nephew, Inc. for return instructions.
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Affected products
5.5 MM Arthrogarde Hip Access Cannula
Model: 72201743
Lot: 50822169, 50834909, 50838788, 50842905, 50846565
Why this matters
Manufacturing error
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: 50822169, 50834909, 50838788, 50842905, 50846565
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 72201743
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?
Manufacturing error
What should consumers do?
Stop using the product immediately. Check the model and lot numbers. Contact Smith & Nephew, Inc. 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. Manufacturing error
When was this product recalled?
This product was recalled on October 2, 2020.
Is the Arthrogarde brand affected by this recall?
Yes, Arthrogarde products are affected by this recall. This recall involves the 5.5 MM Arthrogarde Hip Access Cannula sold in Canada. It's being recalled due to a manufacturing error with the "J-Lock" feature. Stop using the product and follow the return steps in the official notice.