Affected Devices: Alaris® Pump modules, Alaris® Syringe modules, Alaris® PCA modules, Alaris® SpO2 modules and Alaris® PC units (model 8000) manufactured prior to March 26, 2004
Issue: Each Alaris® PC unit (model 8000) and all modules have 2 IUI connectors (left and right). The IUI is used to establish power and communications between the Alaris® PC unit (model 8000) and attached modules. The Grey IUI Connector may fail due to possible physical damage or fluid ingress.
Recall Information and Q&A: For the most current information or answers to questions, please contact the Cardinal Health Recall Center at 800.625.6627.
Adverse Reports: If you have any adverse reports related to the Alaris® System, 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.