Durasul Modular Head recall in Canada: Device compatibility issue
In plain language
This recall involves the Durasul Modular Head, a medical device. It's being recalled because of a device compatibility issue with certain components, which could lead to a reduced range of motion. This reduced range of motion could potentially result in health risks. This recall is intended for healthcare professionals.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Durasul Modular Head
Model: 01.01012.384
Lot: All lots
Why this matters
Reduced range of motion leading to potential health risks
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: All lots
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 01.01012.384
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?
Reduced range of motion leading to potential health risks
What should consumers do?
Contact the manufacturer if you require additional 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. Reduced range of motion leading to potential health risks
When was this product recalled?
This product was recalled on March 15, 2023.
Is the Zimmer GmbH brand affected by this recall?
Yes, Zimmer GmbH products are affected by this recall. This recall involves the Durasul Modular Head, a medical device. It's being recalled because of a device compatibility issue with certain components, which could lead to a reduced range of motion. This reduced range of motion could potentially result in health risks. This recall is intended for healthcare professionals.