Home / Recalls / Medical Devices
CareFusion 303, Inc. recalls Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19; Central programming, monitoring and power supply
Recalled July 6, 2016 · FDA recall Z-2064-2016 · CareFusion 303
Hazard
A patient weight can be populated incorrectly under certain conditions when using the RESTORE feature to restore infusions running on the Alaris LVP module model 8100 and the Alaris Syringe module model 8110. · FDA Class II
Units
69,693 units
Sold at
Distributed US (nationwide) and in Canada.
Description
A patient weight can be populated incorrectly under certain conditions when using the RESTORE feature to restore infusions running on the Alaris LVP module model 8100 and the Alaris Syringe module model 8110.
Product
Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19; Central programming, monitoring and power supply component for the Alaris System.
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →