FDA Drug Recalls

Recalls / Brands / Vivitrol

Vivitrol

4 FDA drug recalls involving brand “Vivitrol”.

DateClassProductFirm
2019-09-26Class IIVivitrol (naltrexone for extended-release injectable suspension) 380 mg/vial. Each Carton Contains: 1) One viaAlkermes, Inc.
2019-08-08Class IIVivitrol (naltrexone for extended-release injectable suspension) 380 mg/vial. Each Carton Contains: 1) One viaAlkermes Inc
2014-03-04Class IIVIVITROL (naltrexone for extended-release injectable suspension); 380 mg vial NDC 65757-300-01; RX Only ManufAlkermes, Inc.
2012-11-06Class IIVIVITROL (naltrexone for extended-release injectable suspension) a) 380 mg vial NDC 65757-303-02, b) 380 mg viAlkermes, Inc.