Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations; does not meet in process specification...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Lloyd Inc. of Iowa directly.
Affected Products
Levothroid (levothyroxine sodium tablets, USP), 300 mcg., 100-count bottles, Rx only, NDC 0456-1328-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.
Quantity: 1,443/100-tablet bottles
Why Was This Recalled?
cGMP Deviations; does not meet in process specification requirements
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lloyd Inc. of Iowa
Lloyd Inc. of Iowa has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report