FDA recall record

Enalapril Maleate Tablets, USP recall — FDA D-1179-2022

CGMP Deviations

Class IIclassification
D-1179-2022official record ID
Jul 13, 2022report date

Recall record at a glance

Official recordD-1179-2022
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmGolden State Medical Supply Inc.
Report dateJul 13, 2022
Recall initiation dateMar 16, 2022
Quantity31,260 bottles
LocationCamarillo, CA, United States

Official product description

Enalapril Maleate Tablets, USP; 10 mg; 90 tablets, NDC 60429-185-90; manufactured by Taro Pharmaceutical Industries, Ltd.; packaged by GSMS, Incorporated, CA.

Why the product was recalled

CGMP Deviations

Distribution information

Nationwide in the U.S: PA, MA, OH, TX, IL, ND, HI

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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