Accord Healthcare recalls 25 mcg levothyroxine tablets due to subpotent drug levels. This may cause ineffective treatment. Check NDC 16729-447-17 and lot D2400679 for affected products.
Subpotent Drug: Assay below the approved specification
Accord Healthcare is recalling 1000-count levothyroxine tablets that may not contain enough active ingredient. This could lead to ineffective treatment for thyroid conditions. Patients should not use these tablets without consulting their doctor.
The tablets may have less active drug than labeled, meaning they don't provide the intended thyroid hormone levels. This could result in ineffective treatment for hypothyroidism. However, the risk is not immediate or life-threatening.
People with a prescription for this thyroid medication who received the recalled batch. Those with untreated hypothyroidism are at higher risk of treatment failure.
Check for NDC 16729-447-17 and lot number D2400679 on the bottle. The product was manufactured by Intas Pharmaceuticals in India and expires February 2026.
Look for NDC 16729-447-17 and lot number D2400679 on the bottle label.
No, the product is not dangerous but may not contain enough active drug for effective treatment.
Check the bottle for NDC 16729-447-17 and lot number D2400679.
Contact your doctor for guidance on alternative treatment options.
We’ve drafted a message you can send Accord Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0519-2025 — Accord Healthcare Accord Healthcare Hello, I own a Accord Healthcare that is covered by recall D-0519-2025 from Accord Healthcare. 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.
