Elitek recalls
Elitek products have been recalled 1 time, most recently on 26 Aug 2020. The recalling company is usually Sanofi-Aventis U.S. The most common reason is potency & assay.
Total recalls1since 2020
Last 12 months0reported
Class I00% of total
Ongoing1latest 26 Aug 2020
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 100%Class III 0 0%
Why elitek is recalled
Companies
Product types
By year
Ongoing elitek recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Elitek (rasburicase) for injection, 5 mg vial recalledElitek | Sanofi-Aventis U.S | Potency & Assay | Nationwide |
All elitek recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Elitek (rasburicase) for injection, 5 mg vial recalledElitek | Sanofi-Aventis U.S | 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.