Hospira Inc. recalls Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32
Recalled July 20, 2016 · FDA recall D-1359-2016 · Hospira
Hazard
Crystallization: Product contains particulate identified to be crystallized active ingredient. · FDA Class II
Units
373,850 tubes
Sold at
Nationwide
Description
Crystallization: Product contains particulate identified to be crystallized active ingredient.
Product
Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →