Bausch Health Companies, Inc.: Drug Recall
Recall #D-0638-2021 · 06/08/2021
Class III: Low Risk
Recall Details
- Recall Number
- D-0638-2021
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- Bausch Health Companies, Inc.
- Status
- Terminated
- Date Initiated
- 06/08/2021
- Location
- Bridgewater, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2,691 bottles
Reason for Recall
Failed Impurities/Degradation Specifications
Product Description
Mephyton (Phytonadione) 5 mg tablets, 100-count tablets, Rx Only, Manufactured for: Valeant Pharmaceuticals North America, LLC, Bridgewater, NJ, 08807, USA, NDC 0187-1704-05.
Distribution Pattern
Nationwide within the United States
Other Recalls by Bausch Health Companies, Inc.
- Class II: Risk 02/02/2024
- Class III: Low Risk 06/08/2021
- Class III: Low Risk 01/07/2021
- Class III: Low Risk 01/07/2021
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.