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FDAFDA · Food and drugs·Recall number D-0359-2022

Cefixime Capsules, 400 mg, 50-count bottles, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ, NDC 67877-584-50

Published January 12, 2022 · Recall initiated: December 21, 2021

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Failed impurities/degradation specifications

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
CEFIXIME
Manufacturer
Ascend Laboratories, LLC
Distributor
USA nationwide.
Lot
Lot #: 20140293, Exp Dec 2021; 20141525, 20141526, 20141527, Exp Mar 2022; 20143019, 20143020, 20143021, 20143022, Exp July 2022; 20144759, 20144760, 20144761, Exp Nov 22
Risk classification
Class II
Area (FDA)
drug
Country
United States

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