CareFusion 303, Inc. recalls Alaris System PC unit, model no. 8000 and 8015. The central programming, monitoring and power supply component for the

Recalled March 29, 2017 · FDA recall Z-1520-2017 · CareFusion 303

Hazard

Reports where the Low Battery alarm and/or the Very Low Battery alarm are not being triggered before the battery is discharged and all infusion channels are stopped. · FDA Class II

Units

613,800 total units (575,221 units in US)

Sold at

Worldwide distribution. US nationwide, Europe, Australia, New Zealand, South Africa, Greater Asia, Middle East, and Canada.

Description

Reports where the Low Battery alarm and/or the Very Low Battery alarm are not being triggered before the battery is discharged and all infusion channels are stopped.

Product

Alaris System PC unit, model no. 8000 and 8015. The central programming, monitoring and power supply component for the Alaris infusion pump System.

Manufacturer(s)

CareFusion 303, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →