Official recall notice
FDA DrugClass IINotable
FDA Recall: Aripiprazole Tablets USP, Rx only, 30 mg, 30 tablets, Marketed by: Ajanta Pharma USA Inc., Bridgewat
- Recall date
- 2026-06-24
- Category
- Drug
- FDA class
- Class II
Why it was recalled
Hazard
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
Recommended action
What to do
6,143 bottles
Product description
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.