Daiichi Sankyo Pharma Development: 8 recalls on record

Recalls filed with 1 agency: FDA (8).

First recall on record: August 6, 2014. Most recent: August 6, 2014.

Risk classification: Class II: 8

Most recent recalls

DateAgencyProduct
August 6, 2014FDAWelchol Tablets (colesevelam HCl) 625 mg, 180 count bottles, Rx Only, Manufactured for: D…D-1505-2014
August 6, 2014FDABenicar HCT Tablets (olmesartan medoxomil, hydrochlorothiazide) 20 mg/12.5 mg, 30 count b…D-1503-2014
August 6, 2014FDABenicar HCT Tablets (olmesartan medoxomil/hydrochlorothiazide) 40 mg/12.5 mg, 30 count bo…D-1507-2014
August 6, 2014FDAAzor Tablets (amlodipine and olmesartan medoxomil) 10 mg*/40 mg, 30 count bottles, Rx Onl…D-1501-2014
August 6, 2014FDABenicar Tablets (olmesartan medoxomil) 40 mg, 30 and 90 count, Rx Only Manufactured for: …D-1506-2014
August 6, 2014FDABenicar Tablets (olmesartan medoxomil) 20 mg, 30 and 90 count, Rx Only Manufactured for: …D-1502-2014
August 6, 2014FDATribenzor Tablets (olmesartan medoxomil/amlodipine/hydrochlorothiazide), 40 mg/5 mg*/25 m…D-1504-2014
August 6, 2014FDABenicar HCT Tablets (olmesartan medoxomil/hydrochlorothiazide) 40 mg/25 mg, 30 and 90 cou…D-1508-2014

Questions about this company

How many recalls does Daiichi Sankyo Pharma Development have?
Recalert has 8 U.S. recalls on record for Daiichi Sankyo Pharma Development, published between August 6, 2014 and August 6, 2014.
What was the most recent Daiichi Sankyo Pharma Development recall?
FDA recall D-1505-2014, published August 6, 2014: Welchol Tablets (colesevelam HCl) 625 mg, 180 count bottles, Rx Only, Manufactured for: Daiichi Sankyo, Inc., Parsippany, NJ 07054 ---NDC 65597-701-18
Which agencies have handled Daiichi Sankyo Pharma Development recalls?
Daiichi Sankyo Pharma Development appears as the recalling firm in recalls from: FDA (8).

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