Major Pharmaceuticals recalls 112 mcg levothyroxine tablets due to subpotent drug levels. This may cause insufficient thyroid hormone. Rx only product. Check NDC 0904-6954-61 for affected lots.
Subpotent Drug
Major Pharmaceuticals is recalling levothyroxine sodium tablets that may not contain enough active ingredient. This could lead to inadequate thyroid hormone levels in people taking the medication. The product is prescription-only and distributed in specific packaging.
The tablets contain less active thyroid hormone than intended. This subpotent drug may not provide the required hormone levels for treatment. It could lead to inadequate thyroid function in patients.
People prescribed levothyroxine who use this specific tablet product. Those with thyroid conditions are most at risk from insufficient hormone levels.
Check for the NDC code 0904-6954-61 on the product packaging. The product is 100 tablets in 10 x 10 blister packs, labeled as Rx only. It was distributed with lot number N02203 and expires September 2026.
Look for the NDC code 0904-6954-61 on the packaging to confirm if this product is affected.
The recall is for subpotent drug levels, which may not provide enough thyroid hormone. The product is not safe for use as intended.
Check the NDC code 0904-6954-61 on the packaging to confirm if this product is affected. If it is, contact your healthcare provider.
The product is 100 tablets in 10 x 10 blister packs with NDC 0904-6954-61. It was distributed with lot number N02203 and expires September 2026.
We’ve drafted a message you can send Major Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0704-2026 — Major Pharmaceuticals Major Pharmaceuticals Hello, I own a Major Pharmaceuticals that is covered by recall D-0704-2026 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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