FDAFDA · Food and drugs·Recall number D-0129-2019
Metoprolol Succinate Extended Release Tablets, USP 50 mg, 100-count bottle, Rx only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, NDC 62037-831-01
Published October 31, 2018 · Recall initiated: October 19, 2018
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
Failed dissolution specifications: Out-of-Specification dissolution test result obtained during routine stability testing.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Teva Pharmaceuticals USA
- Distributor
- U.S.A. Nationwide including Puerto Rico.
- Lot
- Lot # 1220211M, Exp 02/2019
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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