The Recall Desk
ModerateFDA (Drugs)·D-1506-2014·Announced 2014-08-06

Daiichi Sankyo Recalls Benicar Tablets Due to Temperature Abuse During Shipping

Daiichi Sankyo is recalling Benicar Tablets (olmesartan medoxomil) 40 mg because some products were not stored at controlled room temperature during shipping.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II. The hazard involves temperature abuse during shipping, which is a quality control issue without reported illnesses or injuries, fitting the criteria for a moderate severity score.

Plain-English summary

Daiichi Sankyo Pharma Development is recalling Benicar Tablets (olmesartan medoxomil) 40 mg, 30 and 90 count, Rx Only. The recall involves NDC 65597-104-30 and 65597-104-90. The specific lots affected are Lot #0002096 (30 count) and Lot #0002058 (90 count), both with an expiration date of 12/31/2016.

The recall was initiated because various products were not stored at Controlled Room Temperature as per USP guidelines during shipping. This temperature abuse may affect the quality or stability of the medication.

The affected products were distributed nationwide. Consumers and healthcare providers should stop using the recalled lots and contact their pharmacist or healthcare provider for guidance on replacement or alternative treatment.

The recalled product

Product
Benicar Tablets (olmesartan medoxomil) 40 mg, 30 and 90 count, Rx Only Manufactured for: Daiichi Sankyo, Inc., Parsippany, NJ 07054 --- NDC 65597-104-30 and 65597-104-90
Manufacturer
Daiichi Sankyo Pharma Development
Category
Drug — Prescription Medication
Hazard

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • 30 count - Lot #0002096 Exp - 12/31/2016
  • 90 count - Lot #0002058 Exp -12/31/2016

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 8 recalled by Daiichi Sankyo Pharma Development under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 8 products in this recall →

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