Major Pharmaceuticals recalls 100-count levothyroxine tablets due to subpotent drug content. This means the medication may not provide the intended thyroid hormone levels. Consumers should contact the manufacturer for details.
Subpotent Drug
Major Pharmaceuticals is recalling a specific brand of levothyroxine tablets because they may not contain enough active ingredient. This could lead to improper thyroid hormone levels in users, which might require additional medication adjustments.
The tablets contain less active medication than intended, which can result in insufficient thyroid hormone levels. This may cause symptoms like fatigue, weight gain, or depression in users who rely on the medication for treatment.
People prescribed levothyroxine who received this specific product from Major Pharmaceuticals. Those with thyroid conditions are most at risk of needing dose adjustments.
Check for the product name 'Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 100 Tablets (10 x 10 unit dose blisters) per carton'. The NDC code 0904-6952-61 and lot number N02310 (expiring 01/2027) are also indicators.
Verify the NDC code 0904-6952-61 and lot number N02310 on the packaging.
The medication may not contain enough active ingredient (subpotent), which could lead to improper thyroid hormone levels.
Look for the NDC code 0904-6952-61 and lot number N02310 on the packaging.
Contact Major Pharmaceuticals for guidance on next steps; the recall does not require immediate action but may need dose adjustments.
We’ve drafted a message you can send Major Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0703-2026 — Major Pharmaceuticals Major Pharmaceuticals Hello, I own a Major Pharmaceuticals that is covered by recall D-0703-2026 from Major Pharmaceuticals. 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.
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