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.

Tribenzor Tablets (olmesartan medoxomil/amlodipine/hydrochlorothiazide) Recalled by Daiichi Sankyo Pharma Development Due to Temperature Abuse; various products were not stored at...

Date: July 12, 2014
Company: Daiichi Sankyo Pharma Development
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 Daiichi Sankyo Pharma Development directly.

Affected Products

Tribenzor Tablets (olmesartan medoxomil/amlodipine/hydrochlorothiazide), 40 mg/5 mg*/25 mg 30 count bottles, Rx Only Manufactured for: Daiichi Sankyo, Inc., Parsippany, NJ 07054 --- NDC 65597-116-30

Why Was This Recalled?

Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Daiichi Sankyo Pharma Development

Daiichi Sankyo Pharma Development has 8 total recalls tracked by RecallDetector.

Related Recalls

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