Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Phytonadione Tablets 5mg Recalled by Bausch Health Companies, Inc. Due to Failed Impurities/Degradation Specifications:Out of specification during the 24...

Date: January 7, 2021
Company: Bausch Health Companies, Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Bausch Health Companies, Inc. directly.

Affected Products

Phytonadione Tablets 5mg, 30-count bottle, Rx Only, Manufactured For: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC Bridgewater, NJ 08807 USA NDC 68682-170-30

Quantity: 14,089 bottles

Why Was This Recalled?

Failed Impurities/Degradation Specifications:Out of specification during the 24 month stability testing of Impurity D.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Bausch Health Companies, Inc.

Bausch Health Companies, Inc. has 6 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report