D-0503-2023 Class II Terminated

Recalled by RemedyRepack Inc. — Indiana, PA

FDA drug recall D-0503-2023 was initiated by RemedyRepack Inc. on March 20, 2023 and is designated Class II. Reason for recall: cGMP Deviations The recall status is terminated (terminated October 19, 2023).

Recall Details

Product Type
Drugs
Report Date
April 12, 2023
Initiation Date
March 20, 2023
Termination Date
October 19, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity

Product Description

Simvastatin 40 mg tablets, packaged in a) 30-count bottles (NDC 70518-0060-01) and b) 90-count bottles (NDC 70518-0060-00), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701

Reason for Recall

cGMP Deviations

Distribution Pattern

RemedyRepack distributed product to consignees nationwide within the United States

Code Information

Lot # a): J0656821-103122, Exp. Date 11/30/2023; J0638547-080922, Exp. Date 08/31/2023; J0633575-071822, Exp. Date 07/31/2023 Lot #: b): B1965081-111622, Exp. Date 03/31/2025; B1857922-091922, B1765298-071322, B1786319-072922, B1706842-053122, Exp. Date 04/30/2023; B2003311-120822, Exp. Date 04/30/2025; B1955679-111122, Exp. Date 02/28/2025; B1878942-092922, Exp. Date 11/30/2024; B1823203-082622. Exp. Date 10/31/2024; B1706843-053122, Exp. Date 05/31/2023