Fexofenadine Hcl And Pseudoephedrine Hci recalls

Fexofenadine Hcl And Pseudoephedrine Hci products have been recalled 4 times, most recently on 26 Jan 2022. The recalling company is usually Dr. Reddy's Laboratories. The most common reason is potency & assay.

Total recalls4since 2021
Last 12 months0reported
Class I00% of total
Ongoing0latest 26 Jan 2022

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 0 0%Class III 4 100%

Why fexofenadine hcl and pseudoephedrine hci is recalled

Product types

By year

All fexofenadine hcl and pseudoephedrine hci recalls, newest first

4 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIIKroger, Allergy Relief-D, Fexofenadine HCl recalledFexofenadine Hcl And Pseudoephedrine HciDr. Reddy's LaboratoriesPotency & AssayNationwide
DrugCLASS IIIWal-Fex D, Fexofenadine HCl 60mg/Antihistamine recalledFexofenadine Hcl And Pseudoephedrine HciDr. Reddy's LaboratoriesPotency & AssayNationwide
DrugCLASS IIIFexofenadine HCl 60 mg/ Pseudoephedrine HCl USP Allergy & Congestion recalledFexofenadine Hcl And Pseudoephedrine HciDr. Reddy's LaboratoriesPotency & AssayNationwide
DrugCLASS IIIFexofenadine HCl, 60 mg & Pseudoephedrine HCl 120 mg recalledFexofenadine Hcl And Pseudoephedrine HciDr. Reddy's LaboratoriesPotency & AssayNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.