CareFusion 303, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2671-2017)

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 PC Unit, Model 8015

Product Classification:

Class II

Date Initiated: June 12, 2017

Date Posted: July 12, 2017

Recall Number: Z-2671-2017

Event ID: 77077

Reason for Recall:

BD initiated the recall of Alaris PC unit model 8015 after the firm identified five scenarios which can result in the occurrence of Systems Error Code 255-16-275 and can potentially result in interrupted infusions.

Status: Terminated

Product Quantity: 568,283 units

Code Information:

Notification will be distributed to all Alaris PC Unit model 8015 customers with software versions greater than 9.12.

Distribution Pattern:

Worldwide Distribution - USA (nationwide) and to the countries of : Europe, Australia, New Zealand, South Africa, Greater Asia, Middle East, and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated