Home / Recalls / Shilpa Medicare Limited / D-0125-2021

D-0125-2021 Class II Terminated

Recalled by Shilpa Medicare Limited — Polepally, Jadcherla, N/A

Recall Details

Product Type: Drugs
Report Date: December 16, 2020
Initiation Date: December 8, 2020
Termination Date: March 11, 2022
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 4166 bottles

Product Description

Imatinib Mesylate Tablets 400 mg, Rx Only, 30-count Bottle, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals Inc., Manalapan, NJ 07726, NDC 72485-203-30.

Reason for Recall

CGMP Deviations

Distribution Pattern

Nationwide in the U.S.

Code Information

Lot #s: 7S10032A, 7S10034A, Exp. 02/28/2021

Other recalls by Shilpa Medicare Limited

D-0121-2021 Class II — Busulfan Injection 60 mg/10 mL (6 mg/mL), For Intravenous Infusion Only, Must be (December 8, 2020)
D-0126-2021 Class II — Docetaxel Injection USP 160 mg/8mL (20 mg/mL), For Intravenous Infusion Only, Rx (December 8, 2020)
D-0123-2021 Class II — Azacitidine for Injection 100 mg/vial, For Subcutaneous and Intravenous Use Only (December 8, 2020)
D-0124-2021 Class II — Imatinib Mesylate Tablets 100 mg, Rx Only, 90-count Bottle, Manufactured by: Shi (December 8, 2020)
D-0122-2021 Class II — Azacitidine for Injection 100 mg/vial, For Subcutaneous and Intravenous Use Only (December 8, 2020)