FDA recall record

Brimonidine Tartrate Opthalmic Solution 0.2%, 5 mL bottle recall — FDA D-1373-2020

Failed Impurities/Degradation Specification: There is a slow leaching process from the product label on the bottle which may impact the product over the…

Class IIIclassification
D-1373-2020official record ID
Jul 15, 2020report date

Recall record at a glance

Official recordD-1373-2020
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmSOMERSET THERAPEUTICS LLC
Report dateJul 15, 2020
Recall initiation dateJun 4, 2020
Quantity383,437 bottles
LocationSomerset, NJ, United States

Official product description

Brimonidine Tartrate Opthalmic Solution 0.2%, 5 mL bottle, Rx only, Manufactured for: Somerset Therapeutics, LLC Hollywood, FL 33024. Made in India. NDC 70069-231-01

Why the product was recalled

Failed Impurities/Degradation Specification: There is a slow leaching process from the product label on the bottle which may impact the product over the shelf life.

Distribution information

Nationwide

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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