Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Levothyroxine Sodium Tablets Recalled by Alvogen, Inc Due to Sub-Potent Drug: Out of specification for assay at...
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 Alvogen, Inc directly.
Affected Products
Levothyroxine Sodium Tablets, USP 112 mcg, 90 tablets per bottle, Rx Only, Manufactured by Lloyd Inc., Shenandoah, IA, 51601, Distributed by: Alvogen Inc, Pine Brook, NJ 07058, NDC 47781-654-90.
Quantity: 21,276 bottles
Why Was This Recalled?
Sub-Potent Drug: Out of specification for assay at the 24 month interval.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Alvogen, Inc
Alvogen, Inc has 21 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report