FDAFDA · Food and drugs·Recall number D-0631-2017
Nifedipine Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-370-01.
Published April 12, 2017 · Recall initiated: March 7, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Alvogen, Inc
- Distributor
- Nationwide
- Lot
- Lot #: BXH1P51, BXH66D1, BXH1P51A, BXH5ZS1, Exp. 03/2018; BXH1P52, Exp. 05/2018; BXHBKF1A, and BXHB8S1A, Exp. 10/2018.
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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