Levothyroxine sodium tablets distributed by Major Pharmaceuticals have been pulled from shelves nationwide in a Class II recall announced by the Food and Drug Administration. According to Prevention, certain lots of the widely prescribed medication are “subpotent,” meaning they may fail to deliver the full prescribed dose required by patients managing an underactive thyroid or goiter.
FDA Recall Details for Levothyroxine Sodium Tablets
The nationwide recall impacts specific 10-count blister packs and 100-tablet cartons containing dosages ranging from 25 micrograms to 150mcg. According to the Food and Drug Administration, the affected lot numbers feature expiration dates spanning from July 2026 to January 2027. Patients can find the complete list of recalled lot numbers directly on the FDA website to cross-reference with their current prescriptions.
Did you know? Levothyroxine is a synthetic thyroid hormone commonly prescribed to replace or provide extra thyroid hormone, which is normally produced by the thyroid gland to regulate the body’s energy and metabolism.
Expected Health Impacts and Medical Guidance
Health effects linked to receiving a lower dose from subpotent pills are expected to be both temporary and reversible, according to the Food and Drug Administration. According to Prevention, patients who find a match between their medication and the FDA list should contact their doctor or pharmacist immediately. Regulators advise individuals not to stop taking their medication unless specifically instructed to do so by a medical professional.
Frequently Asked Questions
What should I do if my levothyroxine is part of the recall?
Contact your doctor or pharmacist to verify your prescription, but do not stop taking the medication without professional medical advice, according to the Food and Drug Administration.
Which dosages are affected by the Major Pharmaceuticals recall?
The recall covers dosages ranging from 25 micrograms to 150mcg in specific 10-count blister packs and 100-tablet cartons, per Prevention.
When do the affected lots expire?
The expiration dates for the recalled lots stretch from July 2026 to January 2027, according to the Food and Drug Administration.
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