US Drug Recall Register
Class III · Low risk Terminated Initiated Mar 7, 2017 (9 years ago)

Nifedipine Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib

What was recalled

Nifedipine Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-370-01.

Recalling firm
Alvogen, Inc
NDC code
47781-370-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0631-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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