Clinical TopicsNewsPatient SafetyWeb ExclusivesWorkplace Management

FDA orders recall of Baxter infusion pumps

Share

On May 3, the U.S. Food and Drug Administration (FDA) announced that it has ordered Baxter Healthcare Corp. to recall and destroy all of its Colleague Volumetric Infusion Pumps, reimburse customers for the value of the device, and assist in finding a replacement for the customers. FDA cited “longstanding failure” to correct serious problems with the pumps. Read more at and access questions and answers about the recall at http://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm210768.htm

The views and opinions expressed here are those of the author and do not necessarily reflect the opinions or recommendations of the American Nurses Association, the Editorial Advisory Board members, or the Publisher, Editors and staff of American Nurse Journal. This has not been peer reviewed.

cheryl meeGet your free access to the exclusive newsletter of American Nurse Journal and gain insights for your nursing practice.

NurseLine Newsletter

  • Hidden

*By submitting your e-mail, you are opting in to receiving information from Healthcom Media and Affiliates. The details, including your email address/mobile number, may be used to keep you informed about future products and services.

Test Your Knowledge

Which of the following is correct about the stages of sleep?

More Perspectives