Hospira Inc. recalls Diazepam Injection, USP, 5 mg/mL, 10 mL, Multiple-dose Sterile Non-pyrogenic, Fliptop Vial, C-IV, Rx Only, Hospira, Inc.
Recalled September 4, 2013 · FDA recall D-927-2013 · Hospira
Hazard
Lack of assurance of sterility: ineffective crimp on fliptop vials that may result in leaking at the neck of the vials. · FDA Class II
Units
72,300 vials
Sold at
Nationwide and Puerto Rico
Description
Lack of assurance of sterility: ineffective crimp on fliptop vials that may result in leaking at the neck of the vials.
Product
Diazepam Injection, USP, 5 mg/mL, 10 mL, Multiple-dose Sterile Non-pyrogenic, Fliptop Vial, C-IV, Rx Only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-3213-12
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →