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Nicardipine HCl in all strengths, all doses, and all packaging.

FDA Recall #D-0459-2018 — Class II — December 27, 2017

Recall #D-0459-2018 Date: December 27, 2017 Classification: Class II Status: Terminated

Product Description

Nicardipine HCl in all strengths, all doses, and all packaging.

Reason for Recall

Lack of sterility assurance.

Recalling Firm

Pharmedium Services, LLC — Lake Forest, IL

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

Unknown

Distribution

U.S.A. Nationwide

Code Information

All lots remaining within expiry.

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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