FDA recall record

Bryant Ranch Prepack Valsartan 320 mg tablets, 30-count bottles ( NDC 63629-6905-1) recall — FDA D-1028-2018

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Class IIclassification
D-1028-2018official record ID
Aug 8, 2018report date

Recall record at a glance

Official recordD-1028-2018
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBryant Ranch Prepack Inc.
Report dateAug 8, 2018
Recall initiation dateJul 27, 2018
Quantity990 tablets
LocationBurbank, CA, United States

Official product description

Valsartan 320 mg tablets, 30-count bottles ( NDC 63629-6905-1), 90-count bottles (NDC 63629-6905-2), 28-count bottles (NDC 6362-96905-3), Rx Only, Packaged by Bryant Ranch, Burbank, CA 91504.

Why the product was recalled

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Distribution information

Product was distributed in HI, IN, and FL.

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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