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
- Recalling Firm
- Bausch Health Companies, Inc.
- 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.
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