Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), 1000-count bottle, Rx Only, Manufactured f...

FDA Recall #D-0524-2025 — Class II — June 20, 2025

Recall #D-0524-2025 Date: June 20, 2025 Classification: Class II Status: Ongoing

Product Description

Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-456-17

Reason for Recall

Subpotent Drug: Assay below the approved specification

Recalling Firm

ACCORD HEALTHCARE, INC. — Raleigh, NC

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

2,344 bottles

Distribution

Nationwide in the USA

Code Information

Lot #D2300042, Exp Date: 12/31/2025

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated