Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to Subpotent Drug: Assay below the approved specification...

Date: June 20, 2025
Company: ACCORD HEALTHCARE, INC.
Status: Ongoing
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact ACCORD HEALTHCARE, INC. directly.

Affected Products

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

Quantity: 2,344 bottles

Why Was This Recalled?

Subpotent Drug: Assay below the approved specification

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About ACCORD HEALTHCARE, INC.

ACCORD HEALTHCARE, INC. has 17 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report