Baxter Recalls Parenteral Nutrition Injectables
Baxter announced it has initiated a voluntary recall of two lots of Clinimix (amino acid in dextrose) and one lot of Clinimix E (amino acid with electrolytes in dextrose with calcium) injection parenteral nutrition products after complaints of particulate matter found in the products.
Clinimix and Clinimix E are premixed sterile IV parenteral nutrition products that come in multi-chambered containers and are used as a caloric component and as a protein source in a parenteral nutrition program.
The affected product codes are 2B7729 (Lot # P287045, Exp 06/14), 2B7717 (Lot # P275883, Exp 10/13) and 2B7709 (Lot # P285122, Exp 05/14).
If particulate matter is infused, it may result in blockages of blood vessels. This can lead to stroke, heart attack, or damage to other organs such as the kidney or liver. Allergic reactions, local irritation, and inflammation in tissues and organs may also be possible.
Baxter has notified customers and affected products can be returned to Baxter for credit by contacting (888) 229-0001.
For more information call (800) 422-9837 or visit Baxter.com.