Voriconazole recalls
The FDA has published 11 recalls involving Voriconazole since 2012. The latest was reported on 16 Apr 2025. Most were for sterility. Glenmark Pharmaceuticals Inc., USA has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls11since 2012
Last 12 months0reported
Class I00% of total
Ongoing2latest 16 Apr 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 10 91%Class III 1 9%
Why voriconazole is recalled
Companies
By year
Ongoing voriconazole recalls
2 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Voriconazole Tablets 200 mg recalled by Glenmark PharmaceuticalsVoriconazole | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Voriconazole Tablets 50mg recalled by Glenmark PharmaceuticalsVoriconazole | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
All voriconazole recalls, newest first
11 totalShould you stop taking Voriconazole?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.