T7 Cannulated Driver AO recall in Canada: fracture risk
In plain language
This recall involves the T7 Cannulated Driver AO and T7 Driver Solid AO medical devices sold in Canada. They are being recalled because they may fracture, bend, or shear during use. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Contact Zimmer Biomet for a replacement.
- Return the affected product as instructed.
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Affected products
T7 Cannulated Driver AO
Model: 110018531
Lot: More than 10 numbers, contact manufacturer.
T7 Driver Solid AO
Model: 110018541
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Fracture risk
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 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 110018531, 110018541
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?
Fracture risk
What should consumers do?
Stop using the product immediately. Contact Zimmer Biomet for a replacement. Return the affected product 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?
Yes, there may be a health risk. Fracture risk
When was this product recalled?
This product was recalled on April 12, 2019.
Is the Zimmer Biomet brand affected by this recall?
Yes, Zimmer Biomet products are affected by this recall. This recall involves the T7 Cannulated Driver AO and T7 Driver Solid AO medical devices sold in Canada. They are being recalled because they may fracture, bend, or shear during use. Stop using the product and follow the return steps in the official notice.