July 31 (Reuters) - Medical device maker Baxter International has issued an urgent correction for certain software versions of its infusion pumps that deliver fluids into a patient's body, the U.S.

CHICAGO (Reuters) - U.S. health regulators are placing renewed focus on preventing problems associated with infusion pumps, widely used devices that deliver fluids, such as medication and nutrients, ...

After a drawn-out approval process, medical equipment company Baxter International received regulatory clearance for a new infusion pump machine that is expected to help the company capture more of ...

FILE PHOTO: Signage is seen outside of FDA headquarters in White Oak, Maryland (Reuters) -The U.S. Food and Drug Administration (FDA) said on Friday that Becton Dickinson is recalling its Alaris ...

For the fourth time already this month, the FDA has issued a notice formally bestowing a Class I label—denoting a heightened risk of serious injury or death—upon a recall of yet another drug delivery ...

July 31 (Reuters) - Medical device maker Baxter International (BAX.N), opens new tab has issued an urgent correction for certain software versions of its infusion pumps that deliver fluids into a ...