FDA recall record

Dr. Reddy's Laboratories Clocortolone Pivalate Cream, 0.1%, 90-gram tube recall — FDA D-0598-2018

Failed Stability Specifications:Out-of-specification results observed for viscosity during stability testing.

Class IIIclassification
D-0598-2018official record ID
Mar 21, 2018report date

Recall record at a glance

Official recordD-0598-2018
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmDr. Reddy's Laboratories, Inc.
Report dateMar 21, 2018
Recall initiation dateMar 8, 2018
Quantity4,152 tubes
LocationPrinceton, NJ, United States

Official product description

Clocortolone Pivalate Cream, 0.1%, 90-gram tube, Rx only, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, Manufactured by: DPT, Laboratories Ltd. San Antonio, TX 78215, NDC 43598-341-90

Why the product was recalled

Failed Stability Specifications:Out-of-specification results observed for viscosity during stability testing.

Distribution information

Product was distributed Nationwide in the USA.

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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