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Baxter Recalls IV Solutions

  • Date: 01-07-2016 --
  • 01/05/16, PharmTech
  • body: FDA has announced that on Dec. 18, 2016, Baxter International voluntarily recalled two lots of intravenous solutions because of the potential presence of insect particulates. The recall affected lots of 0.9 percent Sodium Chloride Injection, USP, 250 mL VIAFLEX Plastic Container, which is intended for IV use as a source of water and electrolytes and may also be used as a priming solution in hemodialysis procedures, and 70 percent Dextrose Injection (2000 mL) USP, which is indicated as a source of calories and water for hydration.
  • URL: http://multibriefs.com/ViewLink.php?i=568d2be1c1c36