FDA recall D-612-2013

Hospira Inc. · Class II · drug

Product

70% Dextrose Injection USP, 2000 mL, Rx Only, by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7120-07

Reason for recall

Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.

Distribution

Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia

Key facts

Status
Terminated
Initiation date
2012-05-04
Report date
2013-07-03
Termination date
2015-07-17
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-612-2013