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 Alara Pharmaceutical Co Due to Subpotent; 15 month stability

Date: October 29, 2012
Company: Alara Pharmaceutical Co
Status: Terminated
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 Alara Pharmaceutical Co directly.

Affected Products

Levothyroxine Sodium Tablets, USP, 175 mcg in 90 ct bottles, Manufactured by Patheon Puerto Rico Inc., for Alara Pharmaceutical Corp, San Juan, PR

Quantity: 7,432 bottles

Why Was This Recalled?

Subpotent; 15 month stability

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Alara Pharmaceutical Co

Alara Pharmaceutical Co has 1 total recall tracked by RecallDetector.

Related Recalls

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