Nilotinib recalls
Nilotinib products have been recalled 2 times, most recently on 11 Mar 2026. The recalling company is usually Cipla USA. The most common reason is potency & assay.
Total recalls2since 2026
Last 12 months2reported
Class I00% of total
Ongoing2latest 11 Mar 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 0 0%Class III 2 100%
Why nilotinib is recalled
Companies
By year
Ongoing nilotinib recalls
2 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Nilotinib Capsules recalled by Cipla USANilotinib | Cipla USA | Potency & Assay | Nationwide |
| Drug | CLASS III | Nilotinib Capsules recalled by Cipla USANilotinib | Cipla USA | Potency & Assay | Nationwide |
All nilotinib recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Nilotinib Capsules recalled by Cipla USANilotinib | Cipla USA | Potency & Assay | Nationwide |
| Drug | CLASS III | Nilotinib Capsules recalled by Cipla USANilotinib | Cipla USA | 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.