FDA Drug Recalls

Recalls / Active ingredient / Hydromorphone Hydrochloride

Hydromorphone Hydrochloride

9 FDA drug recalls involving the active ingredient “Hydromorphone Hydrochloride” — 4 Class I.

DateClassProductFirm
2018-02-07Class IHydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency FormuPfizer Inc.
2018-02-07Class IHydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency FormuPfizer Inc.
2017-08-22Class IIHYDROmorphone HCl Injection, USP, 2 mg/mL, 1mL Single-use vial, packaged in cartons of 25 vials, Rx only, HospPfizer Inc.
2017-07-26Class IIHydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial. Mfd For: Teva PaHOSPIRA INC, LAKE FOREST
2017-07-26Class IIHydromorphone Hydrochloride Injection, USP, 50 mg/5 mL (10 mg/mL), 5 mL Single Dose Vial.(10 vials per carton HOSPIRA INC, LAKE FOREST
2017-07-26Class IIHydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial per Carton, 100 viHOSPIRA INC, LAKE FOREST
2014-10-01Class IIHydromorphone Hydrochloride Injection, USP, 10 mg/mL, Rx only, packaged in a) 1 mL Single-dose Vial (NDC 0703-Hospira Inc.
2012-08-15Class IHYDROmorphone HCl Injection, USP, 2 mg/mL, 1 mL fill in a 2.5 mL Carpuject prefilled cartridge unit, packaged Hospira Inc.
2012-05-12Class IHYDROmorphone HCl Injection, USP, 1 mg/mL, 1 mL fill in a 2.5 mL Carpuject prefilled cartridge unit, packaged Hospira Inc.