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CareFusion Announces Board of Directors, Progress on Alaris Consent Decree
Date:6/9/2009

sinesses."

CareFusion also announced that the corrective action plan for field remediation of its infusion pumps, which the company submitted to the Food and Drug Administration (FDA) in April as required by the amended consent decree, has been reviewed and found acceptable by the FDA. The company expects to issue a recall notification by June 12 to inform customers who have products affected by the recall, including details on remediation plans. The company recorded an $18 million reserve in its fiscal third quarter for all actions related to the corrective action plan and continues to believe the amount to be sufficient to fulfill its remediation obligations.

An additional requirement of the amended consent decree was completed on June 2, when an independent expert certified that the company's infusion pump operations are in conformity with the Quality System Regulation and certain other provisions of the Federal Food, Drug and Cosmetic Act. The FDA may conduct its own inspection of CareFusion's infusion pump operations within 45 days. The company anticipates it will resume shipping its Alaris(R) PC unit and PCA module by the end of June, subject to 510(k) clearance from the FDA.

"We take our obligation to manufacture safe and effective products very seriously and have worked diligently to implement corrective actions and a new quality system for our infusion pump products," said Dwight Winstead, chief operating officer of CareFusion. "These important efforts will serve us well as we move forward as an independent company, helping to improve patient safety for hospitals around the world."

About CareFusion Corporation

CareFusion Corporation is currently a wholly owned subsidiary of Cardinal Health (NYSE: CAH) and is expected to become a public company from the planned spinoff of Cardinal H
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SOURCE CareFusion Corporation
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