Taperloc Hip System recall in Canada: tissue reaction risk
In plain language
This recall involves various Taperloc Hip System components and other Zimmer Biomet medical devices sold in Canada. They are being recalled because a previous cleaning process could leave elevated levels of bacterial endotoxin and residual debris on the devices. This could result in a local tissue reaction. Consult your healthcare professional for guidance.
What to do
- Consult your healthcare professional if you have received one of these devices.
- Contact Zimmer Biomet for more information.
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Affected products
Specific affected products are listed in the official notice.
Why this matters
Local tissue reaction
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?
Local tissue reaction
What should consumers do?
Consult your healthcare professional if you have received one of these devices. Contact Zimmer Biomet for more information.
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. Local tissue reaction
When was this product recalled?
This product was recalled on October 25, 2019.
Is the Taperloc Hip System brand affected by this recall?
Yes, Taperloc Hip System products are affected by this recall. This recall involves various Taperloc Hip System components and other Zimmer Biomet medical devices sold in Canada. They are being recalled because a previous cleaning process could leave elevated levels of bacterial endotoxin and residual debris on the devices. This could result in a local tissue reaction. Consult your healthcare professional for guidance.