Hospira Inc. recalls Preservative-Free MORPHINE Sulfate Injection, USP, 10 mg/10 mL (1 mg/mL) 10 mL vial, Rx only, HOSPIRA, INC, LAKE FOREST,
Recalled May 8, 2013 · FDA recall D-308-2013 · Hospira
Hazard
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial · FDA Class II
Units
26,100 vials
Sold at
Nationwide and Puerto Rico
Description
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial
Product
Preservative-Free MORPHINE Sulfate Injection, USP, 10 mg/10 mL (1 mg/mL) 10 mL vial, Rx only, HOSPIRA, INC, LAKE FOREST, IL 60045 USA NDC 0409-3815-12
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →