Accord Healthcare recalls 25 mcg levothyroxine tablets with assay below approved levels. This may cause ineffective treatment. Return or consult doctor for replacement.
Subpotent Drug: Assay below the approved specification
Accord Healthcare is recalling 25 mcg levothyroxine tablets that may not contain enough active ingredient. This could lead to ineffective treatment of thyroid conditions. Affected patients should contact their doctor for proper medication.
The tablets may have less active drug than labeled, causing treatment to be less effective. This could lead to uncontrolled thyroid conditions if the medication doesn't work properly.
Patients prescribed levothyroxine who have the specific 90-count bottle with NDC 16729-447-15. Those with thyroid conditions are most at risk from ineffective treatment.
Look for the 90-count bottle labeled 'Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), Rx Only' with NDC 16729-447-15. The product was manufactured by Intas Pharmaceuticals in India with specific lot numbers.
Verify the product label includes NDC 16729-447-15 and the specific lot numbers mentioned in the recall.
Talk to your healthcare provider about alternative medication options if you have the recalled product.
The tablets may have less active drug than labeled, causing treatment to be less effective.
Contact your doctor for alternative medication options. Do not use the recalled product without medical advice.
Yes, the recalled products have lot numbers D2300325 (expiring 01/31/2026) and D2400536 (expiring 02/28/2026).
We’ve drafted a message you can send Accord Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0518-2025 — Accord Healthcare Accord Healthcare Hello, I own a Accord Healthcare that is covered by recall D-0518-2025 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.
