CLASS II ONGOING Drug recall · Reported 26 Mar 2025 · FDA Enforcement Report

Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg) recalled

Mylan Institutional is recalling Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), distributed nationwide in the US. The recall was initiated on 7 Mar 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 3115773, Exp. 03/31/2025
NDC51079-440, 51079-444, 51079-441, 51079-442, 51079-443, 51079-445
Quantity recalled1,068 cartons

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-0291-2025
FDA event ID
96428
Recalling firm
Mylan Institutional, Rockford, IL
Manufacturer
Mylan Institutional Inc.
Classification
Class II
Status
Ongoing
Recall initiated
7 Mar 2025
FDA classified
20 Mar 2025
Reported
26 Mar 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

7 Mar 2025Recall initiated by company
20 Mar 2025Classified by FDA+13 days
26 Mar 2025Published in enforcement report+6 days

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

Reason for recall

Super-Potent Drug: Out of specification potency results were obtained.

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), Rx Only, 100 Unit Dose Blister Cards of 10 (10 cards of 10 tablets each) per carton, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, Made in India, NDC 51079-443-20.

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

Super-Potent Drug: Out of specification potency results were obtained.

Which lots are affected?

Lot 3115773, Exp. 03/31/2025

Where was it sold?

Nationwide in the USA

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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 96428
ReportedClassRecallCompanyReasonWhere
CLASS IILevothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg) recalledLevothyroxine SodiumMylan InstitutionalPotency & AssayNationwide

More recalls from Mylan Institutional

All 24
ReportedClassRecallCompanyReasonWhere
DrugCLASS IILevothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg) recalledLevothyroxine SodiumMylan InstitutionalPotency & AssayNationwide
DrugCLASS IILevothyroxine Sodium Tablets, USP, 137 mcg recalledLevothyroxine SodiumMylan InstitutionalPotency & AssayNationwide
DrugCLASS IILevothyroxine Sodium Tablets, USP, 112 mcg recalledLevothyroxine SodiumMylan InstitutionalPotency & AssayNationwide
DrugCLASS IILevothyroxine Sodium Tablets, USP, 150 mcg recalledLevothyroxine SodiumMylan InstitutionalPotency & AssayNationwide
DrugCLASS IILevothyroxine Sodium Tablets, USP, 100 mcg recalledLevothyroxine SodiumMylan InstitutionalPotency & AssayNationwide

Other Levothyroxine recalls

All 145