LUXA-D recall in Canada: Foreign product found (March 2026)
In plain language
This recall involves LUXA-D capsules sold in Canada. It's being recalled because a foreign product was found inside a capsule in one batch. Consult your healthcare provider before stopping use and follow the steps in the official notice.
What to do
- Stop using the product if affected.
- Verify if your product is from the affected batch.
- Consult your healthcare provider for any health concerns.
- Contact Jamp Pharma if you have questions.
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Affected products
LUXA-D 2000 units capsules
Lot: S2520177
Why this matters
Foreign product inclusion
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: S2520177
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?
Foreign product inclusion
What should consumers do?
Stop using the product if affected. Verify if your product is from the affected batch. Consult your healthcare provider for any health concerns. Contact Jamp Pharma if you have questions.
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. Foreign product inclusion
When was this product recalled?
This product was recalled on March 31, 2026.
Is the Jamp Pharma brand affected by this recall?
Yes, Jamp Pharma products are affected by this recall. This recall involves LUXA-D capsules sold in Canada. It's being recalled because a foreign product was found inside a capsule in one batch. Consult your healthcare provider before stopping use and follow the steps in the official notice.