FDA recall record

Akorn Desoximetasone Gel USP, 0.05% recall — FDA D-1469-2016

Failed impurities/degradation specifications: product was out of specification for unknown impurity at the 9 month stability time point

Class IIIclassification
D-1469-2016official record ID
Aug 31, 2016report date

Recall record at a glance

Official recordD-1469-2016
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAkorn, Inc.
Report dateAug 31, 2016
Recall initiation dateJul 27, 2016
Quantity4,045 units
LocationLake Forest, IL, United States

Official product description

Desoximetasone Gel USP, 0.05%, packaged in 60 gram aluminum tubes, Rx only, Marketed by: VersaPharm Incorporated Marietta, GA 30062, Manufactured by: Ei LLC Kannapolis, NC 28083, NDC 61748-205-60.

Why the product was recalled

Failed impurities/degradation specifications: product was out of specification for unknown impurity at the 9 month stability time point

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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