Recall files available for download:
Alaris® SE Pump (a.k.a. Signature Edition® Infusion System) recall information
Recall Information and Q&A: 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 Cardinal Health Customer Advocacy at 800.854.7128, Option 1, Option 1, then Option 3, or via email at
customerfeedback@cardinalhealth.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.
Consent Decree
