JAMP Senna recall in Canada: May contain excessive yeast and mold
In plain language
This recall involves JAMP Senna tablets sold in Canada. It's being recalled because total counts of yeasts and molds are out of specification. Consult your healthcare provider before stopping use 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 Jamp Pharma Corporation if you have questions.
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Affected products
SENNA Tablet USP ; JAMP Senna ; Jamp - SENNA
Lot: 2A02B3015
Why this matters
Product safety issue due to out-of-specification yeast and mold counts
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: 2A02B3015
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?
Product safety issue due to out-of-specification yeast and mold counts
What should consumers do?
Verify if your product is affected. Consult your healthcare provider prior to discontinuing use. Contact Jamp Pharma Corporation 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. Product safety issue due to out-of-specification yeast and mold counts
When was this product recalled?
This product was recalled on February 5, 2025.
Is the JAMP brand affected by this recall?
Yes, JAMP products are affected by this recall. This recall involves JAMP Senna tablets sold in Canada. It's being recalled because total counts of yeasts and molds are out of specification. Consult your healthcare provider before stopping use and follow the return steps in the official notice.