FDA recall record

Fougera Pharmaceuticals Triamcinolone Acetonide Lotion USP, 0.1%, 60 mL Bottle recall — FDA D-1440-2014

Failed PH Specifications: It has been determined that the pH of the lots recalled, may not meet specification at expiry.

Class IIIclassification
D-1440-2014official record ID
Jul 23, 2014report date

Recall record at a glance

Official recordD-1440-2014
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmFougera Pharmaceuticals Inc.
Report dateJul 23, 2014
Recall initiation dateJul 3, 2014
Quantity111,388 Bottles
LocationMelville, NY, United States

Official product description

Triamcinolone Acetonide Lotion USP, 0.1%, 60 mL Bottle, Rx Only, For Dermatologic Use Only, Not for Ophthalmic Use, E. Fougera & Co, A Division of Fougera Pharmaceuticals Inc., Melville, New York, 11747, NDC 0168-0337-60.

Why the product was recalled

Failed PH Specifications: It has been determined that the pH of the lots recalled, may not meet specification at expiry.

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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