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

Adalat CC (nifedipine) Extended Release Tablets 30 mg, 100-count bottles, Rx only…

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

Adalat CC (nifedipine) Extended Release Tablets 30 mg, 100-count bottles, Rx only, Manufactured for Bayer Healthcare Bayer Healthcare Pharmaceuticals Inc. Whippany, NJ 07901 Manufactured in Germany, NDC 50419-701-05

Recalling firm
Alvogen, Inc
NDC code
50419-701-05
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0628-2017

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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