Why didn’t FDA remove these infusion pumps from health care facilities or from individual customers?
FDA did not require the removal of all Alaris infusion pumps because we are concerned that this could create a shortage of pumps within facilities, for example those that rely heavily on this model and do not have a source of replacement devices. FDA explored all of the options in making this decision. Although not ideal, we believe that this solution best addresses the dual needs of correcting the problem and protecting patient safety. Can I continue to use this infusion pump? Each facility must make this decision individually based on its own inventory and needs. In the busy hospital environment, the additional diligence needed to ensure these infusion pumps are functioning properly is not ideal. If you have the option of using other pumps until this problem is corrected, you may decide to do so. If you do not have other pumps available to you, and you decide to continue using this model pump, you should follow carefully the company’s instructions for proper use. How does Alaris inte
