LFIT CoCr V40 Head recall in Canada: Dissociation risk
In plain language
This recall involves LFIT CoCr V40 Head and Femoral Head COCR LFIT medical devices sold in Canada. They are being recalled because of a higher than expected number of complaints about femoral head/hip stem dissociation. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer for specific lot and serial numbers.
- Follow the manufacturer's instructions for return or replacement.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
LFIT CoCr V40 Head
Model: 6260-9-040, 6260-9-044, 6260-9-140, 6260-9-144
Lot: More than 100 numbers, contact manufacturer.
Femoral Head COCR LFIT
Model: 6260-9-036, 6260-9-136, 6260-9-236, 6260-9-336
Lot: More than 100 numbers, contact manufacturer.
Why this matters
Femoral head/hip stem dissociation
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 100 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 6260-9-036, 6260-9-040, 6260-9-044, 6260-9-136, 6260-9-140, 6260-9-144, 6260-9-236, 6260-9-336
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?
Femoral head/hip stem dissociation
What should consumers do?
Stop using the product immediately. Contact the manufacturer for specific lot and serial numbers. Follow the manufacturer's instructions for return or replacement.
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. Femoral head/hip stem dissociation
When was this product recalled?
This product was recalled on June 1, 2018.
Is the LFIT brand affected by this recall?
Yes, LFIT products are affected by this recall. This recall involves LFIT CoCr V40 Head and Femoral Head COCR LFIT medical devices sold in Canada. They are being recalled because of a higher than expected number of complaints about femoral head/hip stem dissociation. Stop using the product and follow the return steps in the official notice.