Drug recall D-0498-2023

Class II Terminated reported Apr 12, 2023

Product

Atorvastatin 20 mg tablets, packaged in a) 30-count bottles (NDC 70518-1977-00) and b)90-count bottles (NDC 70518-1977-01), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701.

Reason for recall

cGMP Deviations

Lots and codes

Lot #: a) J0659819-110922, Exp. Date 11/30/2023; J0649932-093022, J0649917-093022 Exp. Date 10/31/2023, B2010060-121222, Exp. Date 03/31/24 Lot #: b) B1708575-060122, Exp. Date 05/31/2023; B1879236-092922, Exp. Date 12/31/2023

Recall details

Recalling firm
RemedyRepack Inc., Indiana, PA
Quantity
3,426 bottles
Distribution
RemedyRepack distributed product to consignees nationwide within the United States
Type
Voluntary: Firm initiated
Recall initiated
March 20, 2023
Terminated
October 19, 2023