Accord Healthcare recalls 1000-count levothyroxine tablets due to assay below approved levels. This may result in insufficient thyroid hormone delivery. Consumers should contact the manufacturer for details.
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 inadequate thyroid hormone levels in patients taking the medication.
The tablets have been tested and found to contain less active ingredient than specified. This means they may not provide the intended thyroid hormone dose, potentially leading to insufficient hormone levels in the body.
People prescribed levothyroxine medication who own this specific 1000-count bottle. Those with thyroid conditions are most at risk if the medication doesn't deliver the correct dose.
Check for the 1000-count bottle labeled 'Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), Rx Only'. The product was manufactured by Intas Pharmaceuticals in India with lot number D2300076 and expires December 31, 2025.
Reach out to Accord Healthcare for specific instructions on how to handle the recalled product.
The tablets have been found to contain less active ingredient than specified, which could result in insufficient thyroid hormone delivery.
This is a low-risk situation as the product may not deliver the correct dose but does not pose an immediate safety hazard.
Check for the 1000-count bottle labeled 'Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), Rx Only' with lot number D2300076 and expiration date December 31, 2025.
We’ve drafted a message you can send Accord Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0523-2025 — Accord Healthcare Accord Healthcare Hello, I own a Accord Healthcare that is covered by recall D-0523-2025 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.
