Hospira Inc., A Pfizer Company recalls Levophed norepinephrine bitartrate, injection, USP, 4 mg /4 mL (1 mg/mL),Rx only, Hospira, Inc. Lake Forest, IL --- NDC
Recalled June 21, 2017 · FDA recall D-0898-2017 · Hospira Inc., A Pfizer
Hazard
GMP Deviation; A foreign stopper was observed during packaging of a lot of product. · FDA Class II
Units
(720503A): 43,200 vials, (720603A): 400 vials
Sold at
Nationwide, Canada and Singapore
Description
GMP Deviation; A foreign stopper was observed during packaging of a lot of product.
Product
Levophed norepinephrine bitartrate, injection, USP, 4 mg /4 mL (1 mg/mL),Rx only, Hospira, Inc. Lake Forest, IL --- NDC 0409-3375-04
Manufacturer(s)
Hospira Inc., A Pfizer Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →