CareFusion Alaris Pump Module 8100 Recalled for Dim LED Display Segments
CareFusion 303, Inc. is recalling Alaris Pump Module Model 8100 units because LED display segments may appear dim, potentially affecting the visibility of infusion or patient monitoring values.
- Product
- Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data.
- Category
- Medical Device
- Distribution
- Distributed nationwide