Hospira, Inc. recalls Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-
Recalled April 3, 2013 · FDA recall D-215-2013 · Hospira
Hazard
CGMP Deviations: Shipment of product not approved for release. · FDA Class III
Units
1,296 units
Sold at
NC
Description
CGMP Deviations: Shipment of product not approved for release.
Product
Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
Manufacturer(s)
Hospira, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →