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Drug FDA Class II Ongoing Mislabeling

Levothyroxine Sodium Tablets, USP, Thyro-Tabs, 150mcg, 1000 Tablets, Rx only, Manufactured by: LLOYD, Inc., Shenandoah, IA, 51601 USA, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA, NDC: 47781-662-10.

Alvogen, Inc Published Jan 21, 2026

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 60/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Alvogen, Inc or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets.

Affected products (1)

Levothyroxine Sodium Tablets, USP, Thyro-Tabs, 150mcg, 1000 Tablets, Rx only, Manufactured by: LLOYD, Inc., Shenandoah, IA, 51601 USA, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA, NDC: 47781-662-10.

LEVOTHYROXINE SODIUM

NDC: 47781-640, 47781-643, 47781-646, 47781-649, 47781-651, 47781-654, 47781-657, 47781-659, 47781-662, 47781-665, 47781-668, 47781-671, 47781-640-90, 47781-640-10, 47781-643-90, 47781-643-10, 47781-646-90, 47781-646-10, 47781-649-90, 47781-649-10, 47781-651-90, 47781-651-10, 47781-654-90, 47781-654-10, 47781-657-90, 47781-657-10, 47781-659-90, 47781-659-10, 47781-662-90, 47781-662-10, 47781-665-90, 47781-665-10, 47781-668-90, 47781-668-10, 47781-671-90, 47781-671-10
Lot codes: MHA21825
Code info: Lot # MHA21825, Exp Date: December 31, 2027

Affected areas

Nationwide

Timeline

  1. Initiated
    Dec 31, 2025
  2. Published
    Jan 21, 2026
Recall number
D-0259-2026
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA drug enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.