Phytonadione Tablets recall: Impurity Out of Spec
Phytonadione Tablets, 5 mg, 30-count ablets, Rx only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America…
Why was Phytonadione Tablets recalled?
Failed Impurities/Degradation Specifications
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #:19D013P, Exp Date 07/2021; 20D099P, Exp Date 10/2022
- Product
- Phytonadione Tablets, 5 mg, 30-count ablets, Rx only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America…
- Recalling firm
- Bausch Health Companies, Inc.
- Quantity
- 37,797 bottles
- Distribution
- Nationwide within the United States
- Recall date
- June 30, 2021
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)