CareFusion 303, Inc.: Medical Device Recall in 2025 - (Recall #: Z-1304-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software

Product Classification:

Class I

Date Initiated: February 18, 2025

Date Posted: March 19, 2025

Recall Number: Z-1304-2025

Event ID: 96323

Reason for Recall:

Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).

Status: Ongoing

Product Quantity:

Code Information:

Software v12.5.1 or v12.5.2, and prior versions (4.33, 12.0.1, 12.0.2, 12.1, 12.1.2, 12.3) UDIs: 10885403960123 10885403519666 (10885403960116)

Distribution Pattern:

US: AZ, CA, DC, FL, GA, IL, IN, MI, MO, NC, NJ, NY, OH, OR, PA, SC, TX, UT, VA, WA, WI OUS: None

Voluntary or Mandated:

Voluntary: Firm initiated