Medical device recall in Canada: SICAT Implant V2.0 may cause surgical errors
In plain language
This recall involves SICAT Implant V2.0 software sold in Canada. It's being recalled because incorrect planning data could lead to surgical errors during dental implant procedures. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model numbers if provided.
- Return, repair, or dispose of it as instructed.
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Affected products
SICAT Implant V2.0
Model: SICAT IMPLANT
Lot: Sicat Implant V2.0 software
Why this matters
Surgical error 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: Sicat Implant V2.0 software
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: SICAT IMPLANT
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?
Surgical error risk
What should consumers do?
Stop using the product immediately. Check model numbers if provided. Return, repair, or dispose of it 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. Surgical error risk
When was this product recalled?
This product was recalled on August 14, 2020.
Is the SICAT brand affected by this recall?
Yes, SICAT products are affected by this recall. This recall involves SICAT Implant V2.0 software sold in Canada. It's being recalled because incorrect planning data could lead to surgical errors during dental implant procedures. Stop using the product and follow the return/repair steps in the official notice.