FDA Drug Recalls

Recalls / Active ingredient / Irinotecan Hydrochloride

Irinotecan Hydrochloride

6 FDA drug recalls involving the active ingredient “Irinotecan Hydrochloride.

DateClassProductFirm
2020-06-11Class IIIrinotecan HCL Injection, USP, 100mg/5mL, 5 mL vials, Rx only, Manufactured by: Thymoorgan Pharmazie GmbH, ShiHikma Pharmaceuticals USA Inc.
2020-06-11Class IIIrinotecan HCL Injection, USP, 100mg/5mL, 5 mL vials, Rx only, Manufactured by: Thymoorgan Pharmazie GmbH, ShiHikma Pharmaceuticals USA Inc.
2018-06-08Class IIIrinotecan Hydrochloride Injection, USP, 40 mg/2 mL (20 mg/mL), 1 x 2 mL Single Dose Vial, Rx Only, ManufacturIngenus Pharmaceuticals Llc
2018-06-08Class IIIrinotecan Hydrochloride Injection, USP, 100 mg/5 mL (20 mg/mL), 1 x 5 mL Single Dose Vial, Rx Only, ManufactuIngenus Pharmaceuticals Llc
2013-09-23Class IIIrinotecan Hydrochloride Injection, 100 mg/5 mL (20 mg/mL), 1 x 5 mL Single Dose Vial per carton, Rx only, ManWest-Ward Pharmaceutical Corp.
2013-09-23Class IIIrinotecan Hydrochloride Injection, 40 mg/2 mL (20 mg/mL), 1 x 2 mL Single Dose Vial per carton, Rx only, ManuWest-Ward Pharmaceutical Corp.