CareFusion 303, Inc.: Medical Device Recall in 2024 - (Recall #: Z-2262-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units

Product Classification:

Class II

Date Initiated: May 21, 2024

Date Posted: July 10, 2024

Recall Number: Z-2262-2024

Event ID: 94718

Reason for Recall:

Due to a software issue the PC unit may not connect to the server which could impact wireless data transmission to and from the server.

Status: Ongoing

Product Quantity: 168 software version

Code Information:

UDI: 10885403960123/ Software versions 12.5.1

Distribution Pattern:

US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, WA, WI.

Voluntary or Mandated:

Voluntary: Firm initiated