Esomeprazole Magnesium for Delayed-Release Oral Suspension 40mg, packaged in unit dose packets, R...

FDA Recall #D-0183-2021 — Class II — December 17, 2020

Recall #D-0183-2021 Date: December 17, 2020 Classification: Class II Status: Terminated

Product Description

Esomeprazole Magnesium for Delayed-Release Oral Suspension 40mg, packaged in unit dose packets, Rx only, Manufactured by: Cipla Ltd., Kurkumbh, India, Manufactured for: Cipla USA, Inc. 10 Independence Boulevard, Suite 300 Warren, NJ 07059 NDC 69097-529-34

Reason for Recall

Cross- contamination with other products: The excipient, Crospovidone, NF is contaminated with theophylline

Recalling Firm

CIPLA — Warren, NJ

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

6,491 packets

Distribution

U.S.A. Nationwide

Code Information

Lot #: KA00415, KA00416, Exp 11/2021

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated