← FDA ENFORCEMENT
D-0290-2025Class II

Mylan Institutional, Inc.

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Mylan Institutional, Inc.
Product type
Drug
Status
Ongoing
Report date
2025-03-26
Distribution
Nationwide in the USA
Firm state
IL
Product quantity
347 Cartons
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Validation & Qualification
Reason for recall

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

Product description

Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 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 51079-445-20.

Code / lot info

Lot 3116074, Exp. 09/30/2025

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →