FDA Drug Recalls

Recalls / Class II

Class IID-1178-2022

Product

Enalapril Maleate Tablets, USP; 5 mg; 90 tablets, NDC 60429-184-90; manufactured by Taro Pharmaceutical Industries, Ltd.; packaged by GSMS, Incorporated, CA.

Brand name
Enalapril Maleate
Generic name
Enalapril Maleate
Active ingredient
Enalapril Maleate
Route
Oral
NDCs
60429-183, 60429-184, 60429-185, 60429-186
FDA application
ANDA075657
Affected lot / code info
Lot: GS029041, GS029353, GS02986, 5 mg; 90 tablets, Exp.: 09/2022; Lot: GS030056, GS030869, GS033943, Exp.: 10/2022; Lots: GS034490, GS035197, Exp.:02/2023; Lots: GS035198, Exp.: 03/2023; Lots: GS035596, GS035947, GS036759, GS037400, Exp.: 06/2023; Lots: GS038089, GS038763, GS039559, GS040150, Exp.: 10/2023; Lots: GS040151, GS040708, GS041107, Exp.: 12/2023; Lot: GS041654, Exp.: 03/2024.

Why it was recalled

CGMP Deviations

Recalling firm

Firm
Golden State Medical Supply Inc.
Manufacturer
Golden State Medical Supply, Inc.
Notification channel
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Type
Voluntary: Firm initiated
Address
5187 Camino Ruiz, N/A, Camarillo, California 93012-8601

Distribution

Quantity
9,058
Distribution pattern
Nationwide in the U.S: PA, MA, OH, TX, IL, ND, HI

Timeline

Recall initiated
2022-03-16
FDA classified
2022-07-07
Posted by FDA
2022-07-13
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-1178-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: Enalapril Maleate · FDA Drug Recalls