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FDA Medwatch Alert: CLINIMIX and CLINIMIX E Injection/Baxter: Recall - Particulate Matter in Products

Posted 6 Jan 2014 by Drugs.com

ISSUE: Baxter International and FDA notified health professionals and their medical care organizations of a voluntary recall in the United States of two lots of CLINIMIX and one lot of CLINIMIX E Injection parenteral nutrition products due to complaints of particulate matter found in the products. The affected product codes are 2B7729 (lot P287045, exp 06/14), 2B7717 (lot P275883, exp 10/13) and 2B7709 (lot P28512, exp 05/14). The affected lots were distributed to customers between May 2012 and October 2013. If infused, particulate matter may result in blockages 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. BACKGROUND: CLINIMIX (Amino Acid in Dextrose) Injection and CLINIMIX E (Amino Acid with Electrolytes in ... Read more

Related support groups: Total Parenteral Nutrition, Clinimix Sulfite Free, Clinimix E Sulfite Free

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