Hospira Announces an Expansion of a Nationwide Voluntary Recall of Certain Lots of Liposyn™ and Propofol That May Contain Particulate Matter

FOR IMMEDIATE RELEASE – May 27, 2010 - LAKE FOREST, Ill., - Hospira, Inc. (NYSE: HSP), a global specialty pharmaceutical and medication delivery company, announced today it is voluntarily expanding its March 31, 2010, recall of Propofol Injectable Emulsion 1% and Liposyn™ (Intravenous Fat Emulsion) products which include Liposyn II 10%, Liposyn II 20%, Liposyn III 10%, Liposyn III 20%, and Liposyn III 30% to the consumer or user level. Hospira is conducting the recall because some of the containers may contain particulate matter. The particulate is primarily made up of sub-visible inert stainless steel particles.

The affected lot numbers are shown in the table below:

Hospira initially announced a recall of propofol and Liposyn to its customers on March 31, 2010. The expanded recall announced today affects additional lots of propofol and Liposyn distributed during a wider timeframe to capture all product that might currently be in customer inventories.

The affected lots of Liposyn were distributed between December 2008 and April 2010. The affected lots of propofol were distributed between March 2008 and April 2010. These products were distributed in the United States, Barbados, Canada, Chile, South Korea, Australia, Dominican Republic, Japan, Philippines, Puerto Rico, Uruguay, and the U.S. Virgin Islands. These products are packaged in glass containers. Propofol containers come in 20 mL, 50 mL and 100 mL sizes. Liposyn containers come in 250 mL and 500 mL sizes. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA).

Hospira is undertaking this recall in consideration of the potential for safety issues if the products are administered to patients. Since these particulate contaminants do not dissolve in blood they could potentially act as emboli and impede blood flow. Particulates may also cause mechanical damage to the body and may escalate damage through the Systemic Inflammatory Response Syndrome (SIRS). Restriction in blood supply to tissues could lead to stroke, respiratory failure, kidney failure, liver failure, heart attack and/or death.

Hospira has not received any reports of adverse events related to this issue. The issue was discovered during testing of retain samples. Hospira has implemented improvements to its manufacturing process and is coordinating with the FDA to begin distribution of Liposyn and propofol manufactured under the new process as soon as possible. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using these products.

Anyone with an existing inventory should stop use and distribution and quarantine the product immediately and call Stericycle at 1-877-884-7835 to arrange for the return of these products. For medical inquiries, please contact Hospira Medical Communications at 1-800-615-0187. This phone number is available 24 hours a day, seven days a week.

Any adverse reactions experienced with the use of these products and/or quality problems may also be reported to the FDA’s MedWatch Program by fax at 1-800-FDA-0178, by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787.

Current Propofol Supplies to Remain Unaffected

In response to questions from ASA, FDA officials stated, “The recent Hospira recall is not anticipated to significantly impact current supplies. APP [one of the other propofol manufacturers] is continuing to cover the majority of the market for propofol and these lots being recalled by Hospira were distributed April 2010 and earlier. Hospira has implemented improvements to its manufacturing process and is coordinating with the FDA to begin distribution of propofol manufactured under the new process as soon as possible.”

If hospitals, departments or individuals have any questions or are experiencing difficulties obtaining supplies please contact the FDA Drug Shortage Department.