FDA recall record

American Health Packaging Nabumetone Tablets, USP, 500 mg, 100 Tablets per carton recall — FDA D-1372-2020

Labeling Not Elsewhere Classified: The statement Pharmacist: Dispense with the accompanying Medication Guide was not included on the carton label.

Class IIIclassification
D-1372-2020official record ID
Jul 1, 2020report date

Recall record at a glance

Official recordD-1372-2020
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAmerican Health Packaging
Report dateJul 1, 2020
Recall initiation dateJun 10, 2020
Quantity265 cartons
LocationColumbus, OH, United States

Official product description

Nabumetone Tablets, USP, 500 mg, 100 Tablets per carton (10 tablets x 10 blister cards), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC carton: 60687-374-01, NDC unit dose: 60687-374-11

Why the product was recalled

Labeling Not Elsewhere Classified: The statement Pharmacist: Dispense with the accompanying Medication Guide was not included on the carton label.

Distribution information

Nationwide USA

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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