FDA recall record

Aidarex Pharmaceuticals Phentermine, USP Capsules, 15 mg, 30 count bottles recall — FDA D-1162-2017

Failed Impurities/Degradation Specification; out-of-specification results for individual unknown impurities at the 30 month Room Temperature Retained…

Class IIIclassification
D-1162-2017official record ID
Sep 20, 2017report date

Recall record at a glance

Official recordD-1162-2017
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAidarex Pharmaceuticals LLC
Report dateSep 20, 2017
Recall initiation dateSep 5, 2017
Quantity35 bottles
LocationCorona, CA, United States

Official product description

Phentermine, USP Capsules, 15 mg, 30 count bottles, Rx only, Packaged By: Aidarex Pharmaceuticals, Corona, CA, MFG: KVK-TECH INC. Newtown. PA --- 33261-0361-30

Why the product was recalled

Failed Impurities/Degradation Specification; out-of-specification results for individual unknown impurities at the 30 month Room Temperature Retained Sample stability test

Distribution information

Distributed to the state of CA and NV.

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: E-Mail.

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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