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Isosorbide Dinitrate Tablets, USP 5 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., P...

FDA Recall #D-0259-2019 — Class II — November 2, 2018

Recall #D-0259-2019 Date: November 2, 2018 Classification: Class II Status: Terminated

Product Description

Isosorbide Dinitrate Tablets, USP 5 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-223-00

Reason for Recall

Cross Contamination with Other Products

Recalling Firm

Sandoz Inc — Princeton, NJ

Classification

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

Product Type

Drugs

Product Quantity

7817 bottles

Distribution

Nationwide within the United States

Code Information

Lot #: HZ7896, Exp. 05/2021

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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