# FDA recall Z-1375-2025

> **CareFusion 303, Inc.** · Class II · device recall initiated 2025-02-06.

## Product

BD Pyxis:   Anesthesia Station ES, REF: 327,  MedStation ES, REF: 323,  MedStation ES Tower, REF: 352,  CII Safe ES, REF: 1116-00,  CII Safe ES Desktop PC, REF: 1156-00,  CII Safe ES Desktop PC, Wired SCNR, REF: 107-254-01,  CII Safe ES Desktop PC, W-less SCNR, REF: 107-255-01,  Used with Enterprise Server (ES), REF: 1115-00 with affected Enterprise Server software.

## Reason for recall

Sync timeout may occur between the server and automated dispensing device, due to a server software error which may occur if syncing a large amount of data that takes excessive time, which may cause the dispensing devices to become disconnected from the ES server; dispensing devices will not receive updated information, which may lead to incorrect therapy, and delay in accessing medication.

## Distribution

Worldwide - US Nationwide distribution including in the states of KY, OH, NY, MO, NC, PA, FL, TN, CT, LA, MN, VA, MD, CA, TX, NE, IA, OK, MI, PR, SD, IN, ME, KS, IL, NM, WA, AR, HI, MS, GA, WY, WI, VT, AL, NV, NJ, DC, AZ, MT, AK, OR, CO, NH, MA, SC, ID, UT, ND and the countries of TW, CA, AE, MX, SG, AU, NZ, GB, CH, BH.

## Key facts

- **Recall number:** Z-1375-2025
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-06
- **Report date:** 2025-03-26

- **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-1375-2025

## Citation

> AI Analytics. FDA recall Z-1375-2025. Retrieved 2026-06-29 from https://api.ai-analytics.org/recall/Z-1375-2025. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*