FDAFDA · Food and drugs·Recall number D-0639-2021
Phytonadione Tablets, 5 mg, 30-count ablets, Rx only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA, NDC 68682-170-30
Published June 30, 2021 · Recall initiated: June 8, 2021
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 Impurities/Degradation Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Bausch Health Companies, Inc.
- Distributor
- Nationwide within the United States
- Lot
- Lot #:19D013P, Exp Date 07/2021; 20D099P, Exp Date 10/2022
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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