FDA recall record

Stason Pharmaceuticals Selegiline HCL Tablets USP 5mg, 60- count bottles recall — FDA D-1479-2016

Stason Pharmaceuticals is recalling Selegiline HCl tablets, USP 5mg 60 count bottle due to an out of specification result for dissolution of stability…

Class IIIclassification
D-1479-2016official record ID
Sep 14, 2016report date

Recall record at a glance

Official recordD-1479-2016
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmStason Pharmaceuticals, Inc.
Report dateSep 14, 2016
Recall initiation dateAug 23, 2016
Quantity17,013 units
LocationIrvine, CA, United States

Official product description

Selegiline HCL Tablets USP 5mg, 60- count bottles, Rx only, Manufactured by: Stason Pharmaceuticals, Inc. Irvine, CA 92618 Distributed by: Libertas Pharma, Inc. Montgomery, AL 36117. NDC 51862-146-06

Why the product was recalled

Stason Pharmaceuticals is recalling Selegiline HCl tablets, USP 5mg 60 count bottle due to an out of specification result for dissolution of stability samples.

Distribution information

North Carolina

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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