FDA recall record

Akorn Triamcinolone Acetonide Lotion, USP 0.1%, 60 mL bottle recall — FDA D-0617-2018

Failed Impurities/Degradation Specifications: High out of specification results for an impurity.

Class IIIclassification
D-0617-2018official record ID
Mar 28, 2018report date

Recall record at a glance

Official recordD-0617-2018
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAkorn, Inc.
Report dateMar 28, 2018
Recall initiation dateMar 9, 2018
Quantity4,128 bottles
LocationLake Forest, IL, United States

Official product description

Triamcinolone Acetonide Lotion, USP 0.1%, 60 mL bottle, Rx Only, Marketed by: VersaPharm Incorporated, Marietta, GA 30062; Manufactured by: Ei LLC, Kannapolis, NC 28083, NDC 61748-220-60.

Why the product was recalled

Failed Impurities/Degradation Specifications: High out of specification results for an impurity.

Distribution information

Nationwide in the USA and Puerto Rico

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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