Reported Aug 6, 2014 · Terminated

Tribenzor Tablets (olmesartan medoxomil/amlodipine/hydrochlorothiazide), 40 mg/5 mg*/25 mg 30 count bottles, Rx Only…

Daiichi Sankyo Pharma Development

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Daiichi Sankyo Pharma Development · 399 Thornall St · Edison, NJ · 08837-2236

Is this the product you have?

  • Tribenzor Tablets (olmesartan medoxomil/amlodipine/hydrochlorothiazide), 40 mg/5 mg*/25 mg 30 count bottles
  • Rx Only Manufactured forDaiichi Sankyo, Inc., Parsippany, NJ 07054 --- NDC 65597-116-30
Lot codes and dates
  • Lot #211836 Exp - 11/30/2016

This recall covers 8 products

The agency filed one notice per product. You are reading one of them; the other 7 are below.

Where it was sold

  • Nationwide

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Mar 16, 2015 · Data as of Sep 19, 7:13 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.