CareFusion 303, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1520-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: November 1, 2016

Date Posted: March 29, 2017

Recall Number: Z-1520-2017

Event ID: 75353

Reason for Recall:

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.

Status: Terminated

Product Quantity: 613,800 total units (575,221 units in US)

Code Information:

all units

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated