WB Anatomic Healing Abutment XC recall in Canada: labelling error
In plain language
This recall involves WB Anatomic Healing Abutment XC, a medical device, sold in Canada. It's being recalled because of incorrect labelling on the blister packaging. This could lead to using the wrong abutment with an implant, potentially causing the abutment connection to exceed the implant shoulder.
What to do
- Contact the manufacturer, Institut Straumann Ag, for additional information.
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Affected products
WB Anatomic Healing Abutment XC
Model: 064.4522S, 064.4523S
Lot: All lots
Why this matters
Incorrect medical device application due to labelling error
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: 064.4522S, 064.4523S
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?
Incorrect medical device application due to labelling error
What should consumers do?
Contact the manufacturer, Institut Straumann Ag, for 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. Incorrect medical device application due to labelling error
When was this product recalled?
This product was recalled on April 23, 2025.
Is the Institut Straumann Ag brand affected by this recall?
Yes, Institut Straumann Ag products are affected by this recall. This recall involves WB Anatomic Healing Abutment XC, a medical device, sold in Canada. It's being recalled because of incorrect labelling on the blister packaging. This could lead to using the wrong abutment with an implant, potentially causing the abutment connection to exceed the implant shoulder.