FDA recall record

Topicort (desoximetasone) Topical Spray, 0.25%, 100 mL Bottles recall — FDA D-1370-2015

Failed Impurities/Degradation Specifications: Out of specification results for impurities testing was obtained at the 6 and 9 month time points.

Class IIIclassification
D-1370-2015official record ID
Sep 2, 2015report date

Recall record at a glance

Official recordD-1370-2015
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmTaro Pharmaceuticals, Inc.
Report dateSep 2, 2015
Recall initiation dateAug 5, 2015
Quantity16,320 Bottles
LocationBrampton, N/A, Canada

Official product description

Topicort (desoximetasone) Topical Spray, 0.25%, 100 mL Bottles, Rx Only. Mfd by: Taro Pharmaceuticals, Inc., Brampton, Ontario, Canada, L6T 1C1, Dist by: TaroPharma, Hawthorne, NY 10532. NDC: 51672-5281-7.

Why the product was recalled

Failed Impurities/Degradation Specifications: Out of specification results for impurities testing was obtained at the 6 and 9 month time points.

Distribution information

U.S. 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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