Tribenzor Tablets recall
Tribenzor Tablets (olmesartan medoxomil/amlodipine/hydrochlorothiazide), 40 mg/5 mg*/25 mg 30 count bottles, Rx Only Manufactured for: Daiichi Sankyo…
Why was Tribenzor Tablets recalled?
Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #211836 Exp - 11/30/2016
- Product
- Tribenzor Tablets (olmesartan medoxomil/amlodipine/hydrochlorothiazide), 40 mg/5 mg*/25 mg 30 count bottles, Rx Only Manufactured for: Daiichi Sankyo…
- Recalling firm
- Daiichi Sankyo Pharma Development
- Distribution
- Nationwide
- Recall date
- August 6, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)