Major Pharmaceuticals recalls 150 mcg levothyroxine tablets due to subpotent drug content. This may cause insufficient thyroid hormone levels. Check NDC codes and expiration dates for affected units.
Subpotent Drug
Major Pharmaceuticals is recalling 150 mcg levothyroxine sodium tablets because they contain less active drug than labeled. This could lead to inadequate thyroid hormone levels in patients taking the medication.
The tablets contain less active drug than labeled, which means they may not provide enough thyroid hormone for patients. This could lead to insufficient thyroid hormone levels in those taking the medication.
People prescribed levothyroxine medication by a doctor who own this specific tablet product. Those with thyroid conditions are most at risk from improper dosing.
Check for NDC code 55154-3563-0 (bag) or 0904-6956-61 (blister) on the packaging. The expiration date is July 2026 for both the bag and blister packs.
Look for NDC codes 55154-3563-0 or 0904-6956-61 on the packaging to confirm if your tablets are affected.
The tablets contain less active drug than labeled, which may result in insufficient thyroid hormone levels for patients.
Check for NDC code 55154-3563-0 (bag) or 0904-6956-61 (blister) on the packaging. The expiration date is July 2026 for both the bag and blister packs.
The recall does not specify a remedy, so contact your doctor or pharmacist for guidance on whether to continue using the medication.
We’ve drafted a message you can send Major Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0711-2026 — Major Pharmaceuticals Major Pharmaceuticals Hello, I own a Major Pharmaceuticals that is covered by recall D-0711-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
+ 1 more story