Medical device recall in Canada: Cobalt Chrome Modular Head Component
In plain language
This recall involves the Cobalt Chrome Modular Head Component and 36mm Modular Head. It's being recalled because some products may be mislabeled. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model/serial numbers if provided.
- Return, repair, or dispose of it as instructed.
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Affected products
COBALT CHROME MODULAR HEAD COMPONENT
Model: 163669
Lot: 276760
36MM MODULAR HEAD
Model: 11-363661
Lot: 299340
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: 276760, 299340
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 11-363661, 163669
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?
This recall involves the Cobalt Chrome Modular Head Component and 36mm Modular Head. It's being recalled because some products may be mislabeled. Stop using the product and follow the return/repair steps in the official notice.
What should consumers do?
Stop using the product immediately. Check model/serial numbers if provided. Return, repair, or dispose of it as instructed.
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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on May 1, 2018.