Alembic recalls 4mg extended-release fesoterodine tablets due to diester impurity levels exceeding safety limits. This may pose health risks. Check your prescription bottle for NDC 62332-175-30 and lot number 2405006633.
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
Alembic is recalling 4mg extended-release fesoterodine tablets because they contain too much diester impurity. This could cause health issues if taken as directed. The recall applies to prescription bottles with specific lot numbers and expiration dates.
The tablets contain higher levels of a chemical called diester impurity than allowed by safety standards. This impurity could potentially cause health problems if the medication is taken as intended. The issue is detected through quality control testing during manufacturing.
Prescription patients who have the specific 4mg fesoterodine tablets with NDC 62332-175-30 and lot number 2405006633. Those with the medication still in their prescription or who have taken it recently are most at risk.
Check your prescription bottle for the NDC code 62332-175-30 and lot number 2405006633. The expiration date is March 31, 2026. This product is only available by prescription.
Look for the NDC code 62332-175-30 and lot number 2405006633 on the prescription bottle.
The recall is due to diester impurity levels exceeding safety limits, which could pose health risks. Do not take the affected tablets until you contact your doctor.
Check your prescription bottle for the NDC code 62332-175-30 and lot number 2405006633. If you have the affected product, contact your doctor for guidance.
Look for the NDC code 62332-175-30 and lot number 2405006633 on the prescription bottle. The expiration date is March 31, 2026.
We’ve drafted a message you can send Alembic to request your refund or repair — edit it as you like.
Subject: Recall D-0156-2026 — Alembic Alembic Hello, I own a Alembic that is covered by recall D-0156-2026 from Alembic. 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.
