FDA recall record

Direct Rx Zonisamide Capsules USP, 100 mg, 90-count bottle recall — FDA D-0888-2022

CGMP Deviations: Gaps in the quality system in the Quality Control microbiology laboratory.

Class IIclassification
D-0888-2022official record ID
Jun 1, 2022report date

Recall record at a glance

Official recordD-0888-2022
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmDirect Rx
Report dateJun 1, 2022
Recall initiation dateMay 13, 2022
Quantity16 bottles
LocationDawsonville, GA, United States

Official product description

Zonisamide Capsules USP, 100 mg, 90-count bottle, Rx Only, Packaged and Distributed By: Direct Rx Dawsonville, GA 30534, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430, NDC 61919-775-90

Why the product was recalled

CGMP Deviations: Gaps in the quality system in the Quality Control microbiology laboratory.

Distribution information

Nationwide to the U.S. market

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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