FDA recall D-0832-2016

Hospira Inc. · Class II · drug

Product

Potassium Chloride Injection 20 mEq, 400 mEq/L, Packaged in 50 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7077-14

Reason for recall

Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.

Distribution

US: Nationwide and Singapore

Key facts

Status
Terminated
Initiation date
2016-03-08
Report date
2016-04-27
Termination date
2017-12-06
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0832-2016