Accord Healthcare recalls 1000-bottle supply of 25 mcg levothyroxine tablets due to subpotent content. This may lead to insufficient thyroid hormone levels. Consumers with prescriptions should contact their doctor.
Subpotent
Accord Healthcare is recalling 1000 bottles of 25 mcg levothyroxine sodium tablets because they may not contain enough active ingredient. This could cause thyroid hormone levels to be too low, which might lead to health issues if not properly managed.
Subpotent tablets mean they contain less active levothyroxine than labeled. This could result in insufficient thyroid hormone levels, potentially causing symptoms like fatigue, weight gain, or depression. The risk is not immediate but requires ongoing medical monitoring.
People with a prescription for levothyroxine sodium tablets who received this specific batch from Accord Healthcare. Those with thyroid conditions are most at risk from potential underdosing.
Check for the product name 'Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg)', 1000 bottles, and the lot number D2300323. The expiration date is January 2026. This product is prescription-only and manufactured by Intas Pharmaceuticals Limited in India.
Talk to your healthcare provider about whether you need a new prescription or dosage adjustment.
The tablets may contain less active levothyroxine than labeled (subpotent), which could lead to insufficient thyroid hormone levels.
No, but you should contact your doctor to discuss whether you need a new prescription or dosage adjustment.
The expiration date is January 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-0394-2025 — Accord Healthcare Accord Healthcare Hello, I own a Accord Healthcare that is covered by recall D-0394-2025 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.
