Zydus Pharmaceuticals recalls 1mg Entecavir tablets due to failed impurity testing. This may pose health risks if used improperly. Consumers should contact the manufacturer for details.
Failed impurity/degradation specifications:Out of Specification result for an individual organic impurity
Zydus Pharmaceuticals is recalling 1 mg Entecavir tablets that failed impurity testing. This could pose health risks if the tablets are taken without proper quality control.
The tablets failed impurity testing, meaning they contain an organic impurity that could be harmful if taken. This is a quality issue that may affect the safety of the medication.
People with prescriptions for Entecavir tablets from Zydus Pharmaceuticals (USA) Inc. Those with the specific lot number E409309 are most at risk.
Check for the 1 mg Entecavir tablets in 30-count bottles with lot number E409309. The product was distributed by Zydus Pharmaceuticals (USA) Inc. in the US.
Reach out to Zydus Pharmaceuticals (USA) Inc. for specific instructions on handling the recalled product.
The tablets failed impurity testing, which means they contain an organic impurity that could be harmful if taken.
Contact Zydus Pharmaceuticals (USA) Inc. for specific instructions on handling the recalled product.
Yes, the recalled lot number is E409309.
We’ve drafted a message you can send Zydus Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0002-2026 — Zydus Pharmaceuticals Zydus Pharmaceuticals Hello, I own a Zydus Pharmaceuticals that is covered by recall D-0002-2026 from Zydus Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
