FDAFDA · Food and drugs·Recall number D-0627-2017
Nifedipine Extended-Release Tablets, 30 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-368-01.
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 #: BXH1P22, BXH1P21A, BXH1P21, BXH1P31, BXH1P21B, Exp. 11/2017; BXH6EL1, BXH66A1, BXH6EN1, BXH6EP1, BXH6ER1, Exp. 06/2018; BXH81K1A, BXHBJD1A, Exp. 10/2018
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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