Hospira Inc. recalls 8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 mL, Rx only, Hospira Inc, Lake Forest,
Recalled June 1, 2016 · FDA recall D-0865-2016 · Hospira
Hazard
Presence of Particulate Matter: particulate matter identified as an insect in one vial. · FDA Class I
Units
72,000 units
Sold at
Nationwide
Description
Presence of Particulate Matter: particulate matter identified as an insect in one vial.
Product
8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 mL, Rx only, Hospira Inc, Lake Forest, IL 60045, NDC 0409-6625-02
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →