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We encourage you to report adverse events related to key bounce events by contacting Customer Advocacy at 800.854.7128, extension 7812 or via email at customerfeedback@cardinal.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.
MedWatch Phone: 1.800.FDA.1088
MedWatch Fax: 1.800.FDA.0178
Alaris® SE Pump Recall Information