0.9 % Sodium Chloride Injection, USP, 50  mL VIAFLEX Plastic Container is intended for intravenous use as a source of water and electrolytes. 0.9% Sodium Chloride Injection, USP, 100 mL MINI-BAG Plus Container is indicated as a source of water and electrolytes, and may also be used as a diluent for reconstitution of a powdered drug product packaged in a vial with a 20 mm closure.

The lots being recalled were distributed to customers and distributors in the United States between October 7, 2014 and July 14, 2015. Baxter is directing customers not to use product from the recalled lots. Recalled product should be returned to Baxter for credit by contacting Baxter Healthcare Center for Service at 1-888-229-0001, Monday through Friday, between the hours of 7:00 a.m. and 6:00 p.m., Central Time. Unaffected lots of product are available for replacement.

We partner with surgical teams around the world so they can operate with confidence, precision and speed for a successful outcome to your surgery.

When every moment counts, our therapies help healthcare specialists provide life-sustaining treatment to you or your loved one.

Our forward-looking leadership team is a driving force in ensuring we meet the needs of all our stakeholders – every day and everywhere.

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Nurturing a culture of innovation is critical to delivering on our mission to save and sustain lives. We partner with the healthcare community to continually find more efficient, smarter ways to help solve the world's most pressing healthcare challenges.

Our objective is to accelerate growth by expanding Baxter’s impact across the healthcare spectrum supported by the evolution of our new product pipeline.

Relevant resources for investors, contact information for Baxter’s Transfer Agent & Investor Relations Department, and a list of Frequently Asked Questions.

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From the pharmacy to the bedside, we support you and your healthcare providers with IV medications and infusion technologies designed with safety in mind.

From the pharmacy to the bedside, we help you maximize safety, streamline processes and build cost efficiency throughout the hospital.

Our portfolio of acute, nutritional, renal, hospital and surgical care products helps advance healthcare around the world.

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Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using these drug products.

Our more than 85-year heritage gives us distinct perspective on the needs of patients and caregivers. We lead today by putting those insights to work to deliver new, better healthcare solutions and access to care in the communities where we live and work.

We are committed to doing business the right way, ensuring that we champion our employees, our communities, our customers and patients, and our environment in everything we do.

C-arms are based on X-ray technology and are beneficial for fluoroscopy procedures. More specifically, due to the C-arms technology the system provides the ...

DEERFIELD, Ill., July 17, 2015 – Baxter International Inc. announced today it is voluntarily recalling two lots of intravenous (IV) solutions to the hospital/user level due to the potential presence of particulate matter. The particulate matter in each case was determined to be an insect and was identified as a result of a customer complaint. The matter was identified prior to patient administration and there have been no adverse events associated with this issue reported to Baxter.

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Chronic kidney disease (CKD) is an ongoing journey. While every journey is unique, Baxter is with you every step of the way, providing options to meet your lifestyle needs.

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Monitor your adult and pediatric ambulatory patients with a compact wireless device that delivers the performance of a full-sized patient monitor.

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When medical conditions prevent you from adequately feeding yourself, we provide life-saving clinical nutrition options to help you regain or maintain your health.

Upcoming, featured, and past events and presentations. Also read the latest news on Baxter innovations and initiatives, and follow us on our corporate social media channels.

Adverse reactions or quality problems experienced with the use of these products may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Injecting a product containing particulate matter, in the absence of in-line filtration, may result in blockage of blood vessels, which can result in stroke, heart attack or damage to other organs such as the kidney or liver. There is also the possibility of allergic reactions, local irritation and inflammation in tissues and organs.