FDA Drug Recalls

Recalls / Active ingredient / Diazepam

Diazepam

7 FDA drug recalls involving the active ingredient “Diazepam”.

DateClassProductFirm
2018-07-10Class IIIDiazepam Rectal Gel, 2.5 mg, TWIN PACK that Contains two pre-filled, unit-dose, rectal delivery systems with lValeant Pharmaceuticals North America LLC
2016-06-23Class IIDiazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-3Hospira Inc.
2013-08-16Class IIDiazepam Injection, USP, 5 mg/mL, 10 mL, Multiple-dose Sterile Non-pyrogenic, Fliptop Vial, C-IV, Rx Only, HosHospira Inc.
2013-05-16Class IIDiazepam Injection, USP 5 mg/mL, 10 mL, Multiple-dose fliptop vial, RX only, HOSPIRA, INC. LAKE FOREST, IL 600Hospira Inc.
2013-02-26Class IIDiazepam Injection, USP 5 mg/mL, 10 mL, Multiple-dose fliptop vial, RX only, HOSPIRA, INC. LAKE FOREST, IL 600Hospira Inc.
2012-08-28Class IIDiazepam Injection, USP 5 mg/mL, 10 mL, Multiple-dose fliptop vial, RX only, HOSPIRA, INC. LAKE FOREST, IL 600Hospira Inc.
2012-06-06Class IIDiazepam Injection, USP, 10 mg Automatic, Autoinjector for Buddy Use, 5 mg/mL, 2 mL autoinjector, 15-count autMeridian Medical Technologies a Pfizer Company