PlainRecalls
FDA Drug Low Class III Terminated

Allergy Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, USP, 30 Extended-Release Tablets USP, Distributed By Walmart Inc., Bentonville, AR 72716, Product of India, NDC 49035-273-30.

Reported: December 15, 2021 Initiated: November 12, 2021 #D-0274-2022

Product Description

Allergy Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, USP, 30 Extended-Release Tablets USP, Distributed By Walmart Inc., Bentonville, AR 72716, Product of India, NDC 49035-273-30.

Reason for Recall

Failed dissolution specifications

Details

Units Affected
9,984 cartons
Distribution
USA Nationwide.
Location
Princeton, NJ

Frequently Asked Questions

What product was recalled?
Allergy Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, USP, 30 Extended-Release Tablets USP, Distributed By Walmart Inc., Bentonville, AR 72716, Product of India, NDC 49035-273-30.. Recalled by Dr. Reddy's Laboratories, Inc.. Units affected: 9,984 cartons.
Why was this product recalled?
Failed dissolution specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on December 15, 2021. Severity: Low. Recall number: D-0274-2022.