Voriconazole recalls

Voriconazole products have been recalled 4 times, most recently on 16 Apr 2025. The recalling company is usually Glenmark Pharmaceuticals Inc., USA. The most common reason is manufacturing (cgmp) deviations.

Total recalls4since 2024

Last 12 months0reported

Class I00% of total

Ongoing2latest 16 Apr 2025

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 3 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 4 100%Class III 0 0%

Why voriconazole is recalled

Manufacturing (CGMP) Deviations375%
Packaging Defects125%

Companies

By year

2025375%
2024125%

Ongoing voriconazole recalls

2 active

Reported	Class	Recall	Company	Reason	Where
16 Apr 2025Drug	CLASS II	Voriconazole Tablets 200 mg recalled by Glenmark PharmaceuticalsVoriconazole	Glenmark Pharmaceuticals Inc., USA	Manufacturing (CGMP) Deviations	Nationwide
16 Apr 2025Drug	CLASS II	Voriconazole Tablets 50mg recalled by Glenmark PharmaceuticalsVoriconazole	Glenmark Pharmaceuticals Inc., USA	Manufacturing (CGMP) Deviations	Nationwide

All voriconazole recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
16 Apr 2025Drug	CLASS II	Voriconazole Tablets 200 mg recalled by Glenmark PharmaceuticalsVoriconazole	Glenmark Pharmaceuticals Inc., USA	Manufacturing (CGMP) Deviations	Nationwide
16 Apr 2025Drug	CLASS II	Voriconazole Tablets 50mg recalled by Glenmark PharmaceuticalsVoriconazole	Glenmark Pharmaceuticals Inc., USA	Manufacturing (CGMP) Deviations	Nationwide
9 Apr 2025Drug	CLASS II	Voriconazole Tablets, 50 mg recalled by Amerisource Health ServicesVoriconazole	Amerisource Health Services	Manufacturing (CGMP) Deviations	Nationwide
28 Feb 2024Drug	CLASS II	Voriconazole for Oral Suspension, 40mg/mL recalledVoriconazole	Lupin Pharmaceuticals	Packaging Defects	IL, NJ, OH

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.