FDA Drug Recalls

Recalls / Active ingredient / Pseudoephedrine Hydrochloride

Pseudoephedrine Hydrochloride

6 FDA drug recalls involving the active ingredient “Pseudoephedrine Hydrochloride.

DateClassProductFirm
2022-01-04Class IIIWal-Fex D, Fexofenadine HCl 60mg/Antihistamine & Pseudoephedrine HCl 120mg/Nasal Decongestant, Extended ReleasDr. Reddy's Laboratories, Inc.
2022-01-04Class IIIKroger, Allergy Relief-D, Fexofenadine HCl 60mg/Antihistamine Pseudoephedrine HCl 120mg/Nasal Decongestant, ExDr. Reddy's Laboratories, Inc.
2021-11-12Class IIIFexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Tablets USP Allergy & Congestion, 20 TableDr. Reddy's Laboratories, Inc.
2021-11-12Class IIIAllergy & Congestion Fexofenadine HCl 60 mg & Pseudoephedrine HCl 120 mg Extended-Release Tablets, USP, 20 ExtDr. Reddy's Laboratories, Inc.
2021-11-12Class IIIFexofenadine HCl, 60 mg & Pseudoephedrine HCl 120 mg, Extended Release Tablets USP, Allergy and Congestion, 3Dr. Reddy's Laboratories, Inc.
2021-03-15Class IIBROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE, AND DEXTROMETHORPHAN HYDROBROMIDE SYRUP 10-30-2MG/5ML Cardinal Health Inc.