FDA recall record

Lupin Pharmaceuticals Bimatoprost Ophthalmic Solution 0.03% recall — FDA D-0429-2019

Failed Impurities/Degradation Specifications: OOS results observed in any other individual impurity and total impurities.

Class IIIclassification
D-0429-2019official record ID
Feb 13, 2019report date

Recall record at a glance

Official recordD-0429-2019
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmLupin Pharmaceuticals Inc.
Report dateFeb 13, 2019
Recall initiation dateJan 28, 2019
Quantity9,930 bottles
LocationBaltimore, MD, United States

Official product description

Bimatoprost Ophthalmic Solution 0.03%, packaged in a) 5 mL (NDC 68180-429-02) and b) 7.5 mL (NDC 68180-429-03) bottles, Rx only, Manufactured by: Lupin Limited Pithampur (M.P.) 454 775, INDIA.

Why the product was recalled

Failed Impurities/Degradation Specifications: OOS results observed in any other individual impurity and total impurities.

Distribution information

Nationwide within the United States.

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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