RemedyRepack Inc.: Drug Recall

Recall #D-0502-2023 · 03/20/2023

Class II: Risk

Recall Details

Recall Number
D-0502-2023
Classification
Class II
Product Type
Drug
Recalling Firm
RemedyRepack Inc.
Status
Terminated
Date Initiated
03/20/2023
Location
Indiana, PA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
a) 76 bottles, b)151 bottles

Reason for Recall

cGMP Deviations

Product Description

Rosuvastatin 40mg tablets, packaged in a) 45-count bottles (NDC 70518-1311-01), and b) 90-count bottles (NDC 70518-0484-00), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701.

Distribution Pattern

RemedyRepack distributed product to consignees nationwide within the United States

Other Recalls by RemedyRepack Inc.

View all recalls by RemedyRepack Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.