FDA recall record

KETOCONAZOLE Fougera Ketoconazole Cream 2%, 15g tube recall — FDA D-241-2013

Failed Impurities/Degradation Specifications: Ketoconazole Cream 2% is the subject of a voluntary drug recall by Fougera due to an Out Of Specification…

Class IIIclassification
D-241-2013official record ID
Apr 10, 2013report date

Recall record at a glance

Official recordD-241-2013
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmFougera Pharmaceuticals Inc.
Report dateApr 10, 2013
Recall initiation dateJul 18, 2012
Quantity60,210 units
LocationMelville, NY, United States

Official product description

Fougera Ketoconazole Cream 2%, 15g tube, Rx only, Labeled with E. Fougera & Co., a division of Fougera Pharmaceuticals Inc., Melville, New York 11747, NDC 0168-0099-15

Why the product was recalled

Failed Impurities/Degradation Specifications: Ketoconazole Cream 2% is the subject of a voluntary drug recall by Fougera due to an Out Of Specification result for an unknown degradant product

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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