FDA recall record

Core Pharma Pyridostigmine Bromide Tablets 60 mg, USP recall — FDA D-1062-2013

Failed Stability Specifications: Pyridostigmine Bromide tablets, is being recalled due to an out of specification test result during stablity testing.

Class IIclassification
D-1062-2013official record ID
Oct 2, 2013report date

Recall record at a glance

Official recordD-1062-2013
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCore Pharma LLC
Report dateOct 2, 2013
Recall initiation dateJul 2, 2013
Quantity960 bottles
LocationMiddlesex, NJ, United States

Official product description

Pyridostigmine Bromide Tablets 60 mg, USP Rx Only 100 Tablets, Manufactured and Distributed by: CorePharma, LLC Middlesex, NJ 08846 NDC 64720-128-10 NDC 64720-128-10

Why the product was recalled

Failed Stability Specifications: Pyridostigmine Bromide tablets, is being recalled due to an out of specification test result during stablity testing.

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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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