D-0551-2023 Class II Ongoing

Recalled by Northwind Pharmaceuticals LLC — Indianapolis, IN

Recall Details

Product Type
Drugs
Report Date
May 3, 2023
Initiation Date
March 16, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
a) 230 bottles; b) 22 bottles

Product Description

Glimepiride Tablets, USP 2mg, packaged in a) 30-count bottles (NDC 51655-383-52), and b)90-count bottles (NDC 51655-383-26), Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203.

Reason for Recall

CGMP Deviations

Distribution Pattern

Nationwide with the United States

Code Information

a) Lot #: F106252201, Exp. Date 09/30/2024; F106252301, F106252303, Exp. Date 5/31/2025; F106252304, Exp. Date 07/31/2025 b) Lot #: F106252302, Exp. Date 07/31/2025