FDAClass IIIJune 18, 2025

Levothyroxine Sodium Tablets recall

Levothyroxine Sodium Tablets, USP 112 mcg (0.112mg), 1000 tablets, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540.…

Why was Levothyroxine Sodium Tablets recalled?

Presence of a foreign substance: black hair found embedded in tablet.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #: MLF2401A, Exp 01/31/2026

Product
Levothyroxine Sodium Tablets, USP 112 mcg (0.112mg), 1000 tablets, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540.…
Recalling firm
Macleods Pharmaceuticals Ltd
Quantity
1,344- 1000 count bottles
Distribution
Nationwide in the USA
Recall date
June 18, 2025
Classification
Class III
Status
Ongoing
Agency
FDA (drug)
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