Major Pharmaceuticals recalls 125 mcg levothyroxine tablets due to subpotent drug content. This may not provide adequate thyroid hormone levels. Affected units have specific NDC and lot numbers. Contact for remedy details.
Subpotent Drug
Major Pharmaceuticals is recalling 125 mcg levothyroxine sodium tablets because they may not contain enough active ingredient. This could lead to inadequate thyroid hormone levels in patients who need the medication. The recall affects specific lot numbers and expiration dates.
The tablets may contain less active thyroid hormone than labeled, which could result in insufficient medication levels. This might cause symptoms of hypothyroidism like fatigue, weight gain, or depression. However, the recall does not indicate immediate health risks for most users.
People prescribed levothyroxine medication by a doctor who use the recalled tablets. Those with thyroid conditions are most at risk if they take the medication without proper dosing.
Check for the NDC bag number 55154-3562-0 and blister number 0904-6951-61. The lot numbers are N02266A, N02266B with expiration dates of 11/2026.
Look for the NDC bag number 55154-3562-0 and blister number 0904-6951-61 on the packaging.
The tablets may contain less active thyroid hormone than labeled, which could lead to inadequate medication levels.
Check the product details to see if you have the recalled units. Contact your doctor or the manufacturer for further instructions.
The recall indicates a potential risk of insufficient medication levels, but the manufacturer does not specify immediate health risks for most users.
We’ve drafted a message you can send Major Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0710-2026 — Major Pharmaceuticals Major Pharmaceuticals Hello, I own a Major Pharmaceuticals that is covered by recall D-0710-2026 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.
