PlainRecalls
FDA Drug Moderate Class II Terminated

Allergy Relief D, Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended Release Tablets, USP, 20-count box, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895. Made in India. UPC 0 50428 43023 1

Reported: June 26, 2019 Initiated: June 5, 2019 #D-1388-2019

Product Description

Allergy Relief D, Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended Release Tablets, USP, 20-count box, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895. Made in India. UPC 0 50428 43023 1

Reason for Recall

Testing of Fexofenadine HCl and Pseudoephedrine Failed Impurities/Degradation Specifications: elevated substance results that were reported above or near the specification limit

Details

Units Affected
17,136 20-count units
Distribution
Nationwide in the USA
Location
Cranbury, NJ

Frequently Asked Questions

What product was recalled?
Allergy Relief D, Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended Release Tablets, USP, 20-count box, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895. Made in India. UPC 0 50428 43023 1. Recalled by Sun Pharmaceutical Industries, Inc.. Units affected: 17,136 20-count units.
Why was this product recalled?
Testing of Fexofenadine HCl and Pseudoephedrine Failed Impurities/Degradation Specifications: elevated substance results that were reported above or near the specification limit
Which agency issued this recall?
This recall was issued by the FDA Drug on June 26, 2019. Severity: Moderate. Recall number: D-1388-2019.