Every recall we track for Ajanta Pharma USA Inc — 2 in all — plus the complaints and injury reports the public filed about them.
Ajanta Pharma USA recalls 200mg Fenofibrate capsules due to CGMP deviations. Consumers should check NDC 27241-120-04 and lot # PA02216 for affected units.
Ajanta Pharma recalls 30mg Aripiprazole tablets due to mix-up with Voriconazole tablets. This could lead to incorrect medication use. Check your NDC 27241-056-03 lot PA00805.
