Fexofenadine Hcl And Pseudoephedrine Hci Tablet, Extended Release
FDA Recall NDC 30142-611

FDA Enforcement Report: View Recall Date, Reasons, and Safety Status

Active & Historical Enforcement Reports

The FDA has identified 1 recorded enforcement report(s) associated with Fexofenadine Hcl And Pseudoephedrine Hci (NDC 30142-611). A significant event, classified as Class III, was initiated on Jan 04, 2022 by The Kroger Co.. The reported reason for this action was: "Failed Dissolution Specifications"

This specific recall has a current status of TERMINATED, indicating that the FDA considers the recall process finished or the product successfully recovered.

Reported Recall Events

January 2022 Class III Recall: Failed Dissolution Specifications

Recall Number
Class III Terminated
Reason for Recall
Failed Dissolution Specifications
Initiated
Jan 04, 2022
Reported
Jan 26, 2022
Quantity
11,064 boxes

Recall Profile & Regulatory Data

Event ID
89364
Classification
Class III
Enforcement Status
Terminated
Recalling Firm
Dr. Reddy's Laboratories, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Distribution Pattern
Nationwide in the USA
Termination Date
Oct 20, 2023
Product Description
Kroger, Allergy Relief-D, Fexofenadine HCl 60mg/Antihistamine Pseudoephedrine HCl 120mg/Nasal Decongestant, Extended-Release Tablets USP, 20 tablets per box, NDC 30142-611-14, Distributed by the Kroger Co., Cincinnati, Ohio, 45202, Made in India.
Batch or Lot Expiration Information
Lot# s: AC2000968E, Exp. 8/31/2022; AC2103328A; AC2103330I, Exp. 1/31/2023; AC2106452B, Exp. 3/31/2023.
Affected Packages Involved in this Recall
30142-611-14Product

About FDA Recall Enforcement Reports

FDA recall data documents classified recall actions associated with a product. Most recalls are limited to specific lots, batches, or package configurations rather than every unit of a drug.

If a recall is listed for an NDC, review the affected lot information and package details carefully. Patients and healthcare professionals should confirm whether a specific product in hand matches the lot or package information before assuming it is affected.