Endometrin recall in Canada: Burkholderia contamination
In plain language
This recall involves Endometrin effervescent vaginal tablets sold in Canada. It's being recalled because of potential Burkholderia contamination. Consult your healthcare provider before stopping use or for any health concerns.
What to do
- Verify if your product is affected.
- Contact the recalling firm if you have questions.
- Report any health product related side effects to Health Canada.
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Affected products
Endometrin effervescent vaginal tablets
Lot: AA207A, AB208A
Why this matters
Contamination 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: AA207A, AB208A
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?
Contamination risk
What should consumers do?
Verify if your product is affected. Contact the recalling firm if you have 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. Contamination risk
When was this product recalled?
This product was recalled on June 2, 2023.
Is the Endometrin brand affected by this recall?
Yes, Endometrin products are affected by this recall. This recall involves Endometrin effervescent vaginal tablets sold in Canada. It's being recalled because of potential Burkholderia contamination. Consult your healthcare provider before stopping use or for any health concerns.