FDAFDA · Food and drugs·Recall number D-1508-2014
Benicar HCT Tablets (olmesartan medoxomil/hydrochlorothiazide) 40 mg/25 mg, 30 and 90 count bottles, Rx Only, Manufactured for: Daiichi Sankyo, Inc., Parsippany, NJ 07054 --- NDC 65597-107-30 and NDC 65597-107-90
Published August 6, 2014 · Recall initiated: July 12, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Daiichi Sankyo Pharma Development
- Distributor
- Nationwide
- Lot
- 30 count/Lot #0002108 Exp - 12/31/2016; 90 count/Lot #0002078 Exp - 12/31/2016
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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