Fosaprepitant recalls
Fosaprepitant products have been recalled 2 times, most recently on 31 Jan 2024. The recalling company is usually Fresenius Kabi USA. The most common reason is sterility.
Total recalls2since 2020
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 1 50%Class III 1 50%
Why fosaprepitant is recalled
Companies
Product types
By year
All fosaprepitant recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Fosaprepitant for Injection 150 mg per vial recalledFosaprepitant | Be Pharmaceuticals Ag | Sterility | Nationwide |
| Drug | CLASS III | Fosaprepitant for Injection, 150 mg / vial in a Single-Dose vial recalledFosaprepitant | Fresenius Kabi USA | Labeling Errors | 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.