FDA recall record

Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 10 Tablets (10 x 1) unit dose blisters recall — FDA D-0709-2026

Subpotent Drug

Class IIclassification
D-0709-2026official record ID
Jul 29, 2026report date

Recall record at a glance

Official recordD-0709-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmMajor Pharmaceuticals
Report dateJul 29, 2026
Recall initiation dateJul 13, 2026
QuantityN/A
LocationDublin, OH, United States

Official product description

Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Distributed by Cardinal Health, Dublin, OH 43017. NDC Bag: 55154-3560-0; NDC Blister: 0904-6951-61

Why the product was recalled

Subpotent Drug

Distribution information

Nationwide in the USA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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