APO-Entecavir recall in Canada: Unidentified impurity
In plain language
This recall involves APO-Entecavir 0.5 mg tablets sold in Canada. It's being recalled because an unidentified impurity is out of specification in one lot. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the lot number PY5989.
- Contact your healthcare provider or pharmacist for advice.
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Affected products
APO-Entecavir 0.5 mg Tablet
Lot: PY5989
Why this matters
Unidentified impurity
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: PY5989
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?
Unidentified impurity
What should consumers do?
Stop using the product immediately. Check the lot number PY5989. Contact your healthcare provider or pharmacist for advice.
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. Unidentified impurity
When was this product recalled?
This product was recalled on April 15, 2020.
Is the APO-Entecavir brand affected by this recall?
Yes, APO-Entecavir products are affected by this recall. This recall involves APO-Entecavir 0.5 mg tablets sold in Canada. It's being recalled because an unidentified impurity is out of specification in one lot. Stop using the product and follow the return steps in the official notice.