CareFusion 303, Inc.: Medical Device Recall in 2017 - (Recall #: Z-0950-2017)

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 Pump Module, Model No. 8100 and AIL sensor kits, P/N 147083-102 and P/N 49000221. The Alaris Pump module is a large volume infusion pump offered under the Alaris System. The Alaris Pump module will deliver medication and fluids using IV administration sets for continuous or intermittent delivery through clinically acceptable routes of administration such as intravenous or epidural

Product Classification:

Class I

Date Initiated: December 2, 2016

Date Posted: January 25, 2017

Recall Number: Z-0950-2017

Event ID: 75466

Reason for Recall:

During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion to be interrupted.

Status: Terminated

Product Quantity: 382,635 units

Code Information:

All products manufactured or serviced in the time period October 2011 through June 2015.

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated