PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: June 30, 2021 Initiated: June 8, 2021 #D-0639-2021

Product Description

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

Reason for Recall

Failed Impurities/Degradation Specifications

Details

Units Affected
37,797 bottles
Distribution
Nationwide within the United States
Location
Bridgewater, NJ

Frequently Asked Questions

What product was recalled?
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. Recalled by Bausch Health Companies, Inc.. Units affected: 37,797 bottles.
Why was this product recalled?
Failed Impurities/Degradation Specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on June 30, 2021. Severity: Low. Recall number: D-0639-2021.