Amring Pharmaceuticals recalls Lysteda 650mg tablets due to failed impurities tests. This may pose a risk of harmful substances. Affected lots X220317A and X2:20318A, expiring 09/25.
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Amring Pharmaceuticals is recalling Lysteda 650mg tablets because tests found impurities that could be harmful. This recall affects specific batches made between March 2022 and September 2025. The risk is not immediately dangerous but requires attention to avoid potential harm.
The tablets failed impurities tests, meaning they may contain harmful substances that could cause adverse effects. This is a quality issue that could lead to health risks if the tablets are taken without proper testing.
Prescription users of Lysteda 650mg tablets with the specific batch numbers X220317A and X220318A, expiring September 2025. Patients on anticoagulant therapy are at higher risk due to potential interactions.
Check for the batch numbers X220317A and X220318A on the packaging. The tablets are 650mg, 30-count, prescription-only, with an expiration date of September 2025.
Look for batch numbers X220317A or X220318A on the packaging.
The tablets failed impurities tests, meaning they may contain harmful substances that could cause adverse effects.
Check the batch number on the packaging. If it matches X220317A or X220318A, contact Amring Pharmaceuticals for instructions.
The product is not safe to use as it has failed impurities tests and may contain harmful substances.
We’ve drafted a message you can send Amring Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0871-2023 — Amring Pharmaceuticals Amring Pharmaceuticals Hello, I own a Amring Pharmaceuticals that is covered by recall D-0871-2023 from Amring 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.
