Sanofi Consumer Health Zantac recall in Canada: impurity risk
In plain language
This recall involves Sanofi Consumer Health Zantac 75 mg and 150 mg tablets sold in Canada. It's being recalled because affected lots may contain an impurity called N-nitrosodimethylamine (NDMA). Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the product name and strength.
- Contact your healthcare provider for advice.
- Follow Health Canada's guidance regarding the recall.
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Affected products
Zantac 75 mg Tablet
Lot: All lots
Zantac 150 mg Tablet
Lot: All lots
Why this matters
Impurity 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: All lots
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?
Impurity risk
What should consumers do?
Stop using the product immediately. Check the product name and strength. Contact your healthcare provider for advice. Follow Health Canada's guidance regarding the recall.
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. Impurity risk
When was this product recalled?
This product was recalled on October 18, 2019.
Is the Zantac brand affected by this recall?
Yes, Zantac products are affected by this recall. This recall involves Sanofi Consumer Health Zantac 75 mg and 150 mg tablets sold in Canada. It's being recalled because affected lots may contain an impurity called N-nitrosodimethylamine (NDMA). Stop using the product and follow the return steps in the official notice.