Health & Personal Care
HIGH
FDA DRUG
Lannett NIACIN ER 1,000 mg Recall Affects 46,848 Bottles Nationwide (2025)
Lannett Company, Inc. recalled 46,848 bottles of NIACIN Extended-release Tablets, 1,000 mg, Rx Only, distributed nationwide. The product failed dissolution specifications. Patients and healthcare providers should stop using it immediately and await recall instructions.
Lannett
Failed Dissolution