R3 Acetabular System recall in Canada: May cause locking failure
In plain language
This recall involves specific lots of R3 Acetabular System shells sold in Canada. They are being recalled due to a manufacturing error that may cause an intraoperative locking failure. Patients who have received these devices should consult their healthcare provider for more information.
What to do
- Consult your healthcare provider if you have received an R3 Acetabular System implant.
- Contact Smith & Nephew Inc. for more information if you are a healthcare professional.
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Affected products
Specific affected products are listed in the official notice.
Why this matters
Intraoperative locking failure
Do I have this product?
This recall applies to specific products. Details are listed in the official notice.
Frequently Asked Questions
Why was this product recalled?
Intraoperative locking failure
What should consumers do?
Consult your healthcare provider if you have received an R3 Acetabular System implant. Contact Smith & Nephew Inc. for more information if you are a healthcare professional.
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. Intraoperative locking failure
When was this product recalled?
This product was recalled on May 15, 2020.
Is the R3 Acetabular System brand affected by this recall?
Yes, R3 Acetabular System products are affected by this recall. This recall involves specific lots of R3 Acetabular System shells sold in Canada. They are being recalled due to a manufacturing error that may cause an intraoperative locking failure. Patients who have received these devices should consult their healthcare provider for more information.