Accord Healthcare recalls 1000 bottles of Levothyroxine Sodium Tablets (50 mcg) 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 Levothyroxine Sodium Tablets (50 mcg) because they may contain less active ingredient than labeled. This could cause your thyroid hormone levels to be too low, leading to health issues if not properly managed.
Subpotent means the tablets contain less active thyroid hormone than labeled. This could result in insufficient hormone levels in your body, potentially causing symptoms like fatigue, weight gain, or depression. The risk is low but requires medical monitoring.
People with a prescription for Levothyroxine Sodium Tablets (50 mcg) who own the recalled product. Those with thyroid conditions are most at risk if the medication doesn't provide enough hormone.
Check for the product name 'Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg)' on the label. The product was sold in 1000-bottle packages with NDC 16729-448-17 and lot number D2400547.
Contact your doctor to confirm if you have the recalled product and discuss alternative treatment options.
The product may contain less active ingredient than labeled, so it's not safe to use without medical supervision.
Look for the product name 'Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg)' with NDC 16729-448-17 and lot number D2400547.
Contact your doctor to discuss alternative treatment options and whether you need to stop using the product.
We’ve drafted a message you can send Accord Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0395-2025 — Accord Healthcare Accord Healthcare Hello, I own a Accord Healthcare that is covered by recall D-0395-2025 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.
