FDA recall record

Taro Pharmaceuticals U.S.A ¿Topicort (desoximetasone) Cream USP, 0.05% recall — FDA D-0950-2016

Subpotent Drug

Class IIIclassification
D-0950-2016official record ID
Jun 8, 2016report date

Recall record at a glance

Official recordD-0950-2016
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmTaro Pharmaceuticals U.S.A., Inc.
Report dateJun 8, 2016
Recall initiation dateMar 31, 2016
Quantity62,800 Tubes
LocationHawthorne, NY, United States

Official product description

¿Topicort (desoximetasone) Cream USP, 0.05%, Packaged in 5 g Tubes, Professional Sample Only, Rx Only. Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: TaroPharma a division of Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532. NDC: 51672-5205-5.

Why the product was recalled

Subpotent Drug

Distribution information

U.S. Including: CA, CT, MA, MD, NY, NJ, OK, TX, and WA

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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