FDA recall record

Bausch Health Companies Phytonadione Tablets 5mg, 30-count bottle recall — FDA D-0244-2021

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

Class IIIclassification
D-0244-2021official record ID
Feb 3, 2021report date

Recall record at a glance

Official recordD-0244-2021
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBausch Health Companies, Inc.
Report dateFeb 3, 2021
Recall initiation dateJan 7, 2021
Quantity14,089 bottles
LocationBridgewater, NJ, United States

Official product description

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

Why the product was recalled

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

Distribution information

Distributed Nationwide in the USA

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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