Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

BD Alaris Systems Manager Recalled by CareFusion 303, Inc. Due to Software issue that may result in outdated automated...

Date: February 18, 2025
Company: CareFusion 303, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact CareFusion 303, Inc. directly.

Affected Products

BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software

Why Was This Recalled?

Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).

Where Was This Sold?

This product was distributed to 21 states: AZ, CA, FL, GA, IL, IN, MI, MO, NJ, NY, NC, OH, OR, PA, SC, TX, UT, VA, WA, WI, DC

Affected (21 states)Not affected

About CareFusion 303, Inc.

CareFusion 303, Inc. has 163 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report