Atlantiscan recall in Canada: Broken vials
In plain language
This recall involves Atlantiscan Fludeoxyglucose 18F solution sold in Canada. It's being recalled because the vials may be broken. Consult your healthcare provider and follow the return steps in the official notice.
What to do
- Verify if your product is affected.
- Consult your healthcare provider prior to discontinuing use.
- Contact the recalling firm with any questions.
- Report any health product related side effects to Health Canada.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Atlantiscan Fludeoxyglucose 18F Solution
Lot: F071025
Why this matters
Broken vials
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: F071025
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?
Broken vials
What should consumers do?
Verify if your product is affected. Consult your healthcare provider prior to discontinuing use. Contact the recalling firm with any questions. Report any health product related side effects to Health Canada.
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. Broken vials
When was this product recalled?
This product was recalled on October 10, 2025.
Is the Atlantiscan brand affected by this recall?
Yes, Atlantiscan products are affected by this recall. This recall involves Atlantiscan Fludeoxyglucose 18F solution sold in Canada. It's being recalled because the vials may be broken. Consult your healthcare provider and follow the return steps in the official notice.