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Popular Thyroid Medication Recalled Nationwide, FDA Warns
The FDA said the Class II recall covers tablets that may cause temporary, reversible health effects in patients with thyroid conditions.
- The FDA initiated a nationwide recall for specific lots of levothyroxine sodium tablets distributed by Major Pharmaceuticals due to manufacturing concerns affecting thyroid medication supplies.
- Tablets were found to be "subpotent," meaning they deliver less medication than intended, prompting The FDA to designate the recall Class, indicating potential for temporary, reversible health effects.
- Affected tablets were packaged in 10-count blister packs, sold individually or bundled into cartons containing 10 packs, allowing consumers to identify recalled lots using specific lot numbers and expiration dates.
- Families using thyroid medication should check their medicine cabinets for affected lots, and patients discovering recalled tablets must consult a doctor or pharmacist before taking further action.
- Patients should not discontinue medication unless directed by a healthcare provider, as suddenly stopping treatment can cause ill effects, making professional guidance essential for safe management.
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Often-Prescribed Thyroid Drug Recalled Across the US
A nationwide recall has been issued for a type of thyroid medication over potency issues, according to a notice published by the Food and Drug Administration (FDA) this week. The recalled medication is levothyroxine sodium and includes tablets in different counts and different strengths, the notice said. The FDA said it was recalled because it’s a “subpotent drug,” without elaborating. Major Pharmaceuticals, an Ohio-based company, issued the rec…
·New York, United States
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Total News Sources29
Leaning Left0Leaning Right1Center28Last UpdatedBias Distribution97% Center
Bias Distribution
- 97% of the sources are Center
97% Center
C 97%
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