Atlantis IO Flo-S Kits recall in Canada: performance issue
In plain language
This recall involves Atlantis IO Flo-S Kits A04B and A04S sold in Canada. They are being recalled because a defect in the thread area can prevent proper engagement with an abutment. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Atlantis Io Flo-S Kits A04b And A04s
Model: 10488578, 10505543, 10512084, 10515863, 10544044, 10556741
Lot: 68020033, 68020034
Why this matters
Performance issue
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: 68020033, 68020034
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 10488578, 10505543, 10512084, 10515863, 10544044, 10556741
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?
Performance issue
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. Performance issue
When was this product recalled?
This product was recalled on August 6, 2025.
Is the Dentsply Implants Manufacturing Gmbh brand affected by this recall?
Yes, Dentsply Implants Manufacturing Gmbh products are affected by this recall. This recall involves Atlantis IO Flo-S Kits A04B and A04S sold in Canada. They are being recalled because a defect in the thread area can prevent proper engagement with an abutment. Healthcare professionals should contact the manufacturer for more information.