For the most current information or answers to questions, please contact our Call Center dedicated to the Alaris® SE pump recall at 877.552.4922.
Adverse Reports:
If you have any adverse reports related to the Alaris® SE pump please use our main business line to contact CareFusion Customer Advocacy at 800.854.7128, Option 1, Option 1, then Option 3, or via email at customerfeedback@carefusion.com.
We also encourage you to report adverse events related to key bounce directly to MedWatch, the FDA’s voluntary reporting program. You may submit reports to MedWatch, Food & Drug Administration, 5600 Fishers Lane, Rockville, MD 20857-9787 or online at http://www.fda.gov/medwatch/report.htm.
