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Hospira to Standardize Intravenous (I.V.) Administration Sets Portfolio to Non-DEHP
Date:5/14/2010

tified applications. Hospira's continued transition to non-DEHP will help hospitals align with the recommendations of the FDA notification by providing non-DEHP medication delivery sets designed for use with neonates, and additional options for use with blood, and drugs and solutions that contain lipid (fat) – all of which are product areas identified in the notification.

The I.V. administration sets in Hospira's non-DEHP product line are manufactured with the plasticizer TOTM (tri-octyl trimellitate). TOTM has been used for decades in the manufacture of medical devices.

About Hospira

Hospira, Inc. is a global specialty pharmaceutical and medication delivery company dedicated to Advancing Wellness. As the world leader in specialty generic injectable pharmaceuticals, Hospira offers one of the broadest portfolios of generic acute-care and oncology injectables, as well as integrated infusion therapy and medication management solutions. Through its products, Hospira helps improve the safety, cost and productivity of patient care. The company is headquartered in Lake Forest, Ill., and has approximately 13,500 employees. Learn more at www.hospira.com.

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A Caution Concerning Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding Hospira's goals and strategy. Hospira cautions that these forward-looking statements
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