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Nifedipine, extended-release tablets, 90mg 100 count blister pack, Rx only, Distributed by: GREE...

FDA Recall #D-737-2014 — Class II — November 1, 2013

Recall #D-737-2014 Date: November 1, 2013 Classification: Class II Status: Terminated

Product Description

Nifedipine, extended-release tablets, 90mg 100 count blister pack, Rx only, Distributed by: GREENSTONE LLC, Pespack, NJ,07977, NDC 59762-6692-8

Reason for Recall

Labeling: Incorrect or Missing Lot and/or Exp Date: Greenstone LLC is recalling Nifedipine Extended Release tablets (90mg). The expiration date on the package is 48 months instead of 36 months.

Recalling Firm

Greenstone Llc — Peapack, NJ

Classification

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

Product Type

Drugs

Product Quantity

21600 tablets

Distribution

Nationwide

Code Information

V110079

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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