Lupin Pharmaceuticals recalls Tydemy tablets due to stability and impurity failures. Affected lots may have inactive content and impurities that could pose risks. Contact for details.
Failed Stability Specification and Failed Impurities/Degradation Specifications: out of specification for inactive content ascorbic acid and MTHFRC-7impurity test
Lupin Pharmaceuticals is recalling Tydemy birth control tablets because they failed stability and impurity tests. This means the tablets might contain unsafe levels of inactive ingredients or impurities that could affect safety.
The tablets failed stability and impurity tests, meaning they may have unsafe levels of inactive ingredients like ascorbic acid or impurities that could affect safety. This could lead to potential health risks if the tablets are used as intended.
Women who have purchased Tydemy tablets from the specified lots are affected. Those using the product for birth control are most at risk.
Check the product label for the lot numbers L200183 (expires 1/2024) or L201560 (expires 9/2024). The tablets come in blister packs of 28 tablets per blister, with a carton of 3 blisters.
Look for the lot numbers L200183 or L201560 on the packaging to confirm if your tablets are affected.
Lupin Pharmaceuticals is recalling Tydemy birth control tablets due to failed stability and impurity tests.
Check the lot numbers L200183 (expires 1/2024) or L201560 (expires 9/2024) on the packaging.
The recall record does not specify a remedy, so contact Lupin Pharmaceuticals for further instructions.
We’ve drafted a message you can send Lupin to request your refund or repair — edit it as you like.
Subject: Recall D-1081-2023 — Lupin Lupin Hello, I own a Lupin that is covered by recall D-1081-2023 from Lupin. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.