# FDA recall Z-2262-2024

> **CareFusion 303, Inc.** · Class II · device recall initiated 2024-05-21.

## Product

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

## 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.

## Distribution

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.

## Key facts

- **Recall number:** Z-2262-2024
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-21
- **Report date:** 2024-07-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2262-2024

## Citation

> AI Analytics. FDA recall Z-2262-2024. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-2262-2024. Source: US FDA. Licensed CC0.

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