CareFusion 303, Inc.: Medical Device Recall in 2016 - (Recall #: Z-2879-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Alaris Syringe Module Model 8110 with software version 9.15 The Alaris Syringe Pump module is part of the Alaris System. The syringe pump delivers fluids in a manner similar to current syringe pumps on the market. Up to four Alaris Syringe pump modules can be connected to the Alaris PC unit which is the central programming, monitoring and power supply component for the Alaris System. The syringe pump uses standard, single-use administration sets and syringes with luer-lock connectors.

Product Classification:

Class II

Date Initiated: August 8, 2016

Date Posted: October 5, 2016

Recall Number: Z-2879-2016

Event ID: 74508

Reason for Recall:

A software anomaly with the Alaris Syringe module software version 9.15 may cause an infusion to unexpectedly stop when the Syringe module is transitioning from one rate to another.

Status: Terminated

Product Quantity: 12,000 units

Code Information:

Software version 9.15

Distribution Pattern:

Worldwide Distribution: US(nationwide) and countries of: Canada, Australia and United Arab Emirates.

Voluntary or Mandated:

Voluntary: Firm initiated