CareFusion 303, Inc.: Medical Device Recall in 2012 - (Recall #: Z-2076-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only.

Product Classification:

Class I

Date Initiated: May 25, 2012

Date Posted: August 1, 2012

Recall Number: Z-2076-2012

Event ID: 62007

Reason for Recall:

The recall was initiated because the Alaris PC unit model 8015 has a component on the PC unit power supply board that is causing an error code(120.4630) "System Error" or "Missing Battery Error" at start up. The error code is accompanied by both an audible alarm and visual error messages on the PC unit screen.

Status: Terminated

Product Quantity: 112,912 units total (106,888 units in US)

Code Information:

not available

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated