CLASS II ONGOING Drug recall · Reported 21 Jan 2026 · FDA Enforcement Report

Levothyroxine Sodium Tablets, USP, Thyro-Tabs, 150mcg recalled

Alvogen is recalling Levothyroxine Sodium Tablets, USP, Thyro-Tabs, 150mcg, distributed nationwide in the US. The recall was initiated on 31 Dec 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # MHA21825, Exp Date: December 31, 2027

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0259-2026
FDA event ID
98225
Recalling firm
Alvogen, Morristown, NJ
Classification
Class II
Status
Ongoing
Recall initiated
31 Dec 2025
FDA classified
14 Jan 2026
Reported
21 Jan 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Packaging Defects

Timeline

31 Dec 2025Recall initiated by company
14 Jan 2026Classified by FDA+14 days
21 Jan 2026Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

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.

Where it was distributed

US Nationwide.

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Lot # MHA21825, Exp Date: December 31, 2027

Where was it sold?

US Nationwide.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 2 Oct 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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