PlainRecalls
FDA Drug Moderate Class II Terminated

Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended-Release Tablets, USP, Allergy & Congestion, 20-count box.Distributed by: Walgreen Co. 200 Wilmore Rd. Deerfield, IL 40015. Made in India UPC 3 11917 19453 0

Reported: June 26, 2019 Initiated: June 5, 2019 #D-1390-2019

Product Description

Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended-Release Tablets, USP, Allergy & Congestion, 20-count box.Distributed by: Walgreen Co. 200 Wilmore Rd. Deerfield, IL 40015. Made in India UPC 3 11917 19453 0

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
17,904 20-count units
Distribution
Nationwide in the USA
Location
Cranbury, NJ

Frequently Asked Questions

What product was recalled?
Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended-Release Tablets, USP, Allergy & Congestion, 20-count box.Distributed by: Walgreen Co. 200 Wilmore Rd. Deerfield, IL 40015. Made in India UPC 3 11917 19453 0. Recalled by Sun Pharmaceutical Industries, Inc.. Units affected: 17,904 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-1390-2019.