Hospira Inc. recalls Potassium Chloride for Inj. Concentrate, USP, 40 mEq (2 mEq/mL), 20 mL Single-dose Fliptop Vial, For IV use, Rx only, H
Recalled April 30, 2014 · FDA recall D-1261-2014 · Hospira
Hazard
Presence of Particulate; red and black particulate within the solution and embedded within the plastic vial identified as iron oxide · FDA Class II
Units
255,900 vials
Sold at
Nationwide
Description
Presence of Particulate; red and black particulate within the solution and embedded within the plastic vial identified as iron oxide
Product
Potassium Chloride for Inj. Concentrate, USP, 40 mEq (2 mEq/mL), 20 mL Single-dose Fliptop Vial, For IV use, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →