Fexofenadine Hydrochloride recalls
Fexofenadine Hydrochloride products have been recalled 2 times, most recently on 31 Jan 2024. The recalling company is usually SUN Pharmaceutical Industries. The most common reason is sterility.
Total recalls2since 2023
Last 12 months0reported
Class I00% of total
Ongoing0latest 31 Jan 2024
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 100%Class III 0 0%
Why fexofenadine hydrochloride is recalled
Companies
Product types
By year
All fexofenadine hydrochloride recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Fexofenadine Hydrochloride Tablets, USP 180mg recalledFexofenadine Hydrochloride | SUN Pharmaceutical Industries | Sterility | Nationwide |
| Drug | CLASS II | Fexofenadine Hydrochloride Tablets, 180 mg recalled by L. PerrigoFexofenadine Hydrochloride | L. Perrigo | Potency & Assay | Nationwide |
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.