Fulvestrant recalls
Fulvestrant products have been recalled 2 times, most recently on 24 Aug 2022. The recalling company is usually Glenmark Pharmaceuticals Inc., U. The most common reason is potency & assay.
Total recalls2since 2021
Last 12 months0reported
Class I00% of total
Ongoing0latest 24 Aug 2022
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 fulvestrant is recalled
Companies
Product types
By year
All fulvestrant recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Fulvestrant Injection 250mg/ (50 mg/mL) recalledFulvestrant | Zydus Pharmaceuticals (USA) | Potency & Assay | Nationwide |
| Drug | CLASS II | Fulvestrant Injection 250 mg recalled by Glenmark PharmaceuticalsFulvestrant | Glenmark Pharmaceuticals Inc., U | Sterility | 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.