# FDA recall Z-1550-2025

> **CareFusion 303, Inc.** · Class II · device recall initiated 2025-03-11.

## Product

BD Pyxis MedBank CUBIE Replenishment Station    Product / Material ID  BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P /	155141-01  BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P /	155140-01  BD PYXIS MEDBANK TWR MN CR-12HH-1FH /	155142-01  BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P /	155143-01  BD PYXIS MEDBANK TWR MN CR-14HH-P /	155144-01  BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM / 	155145-01  BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P /	155156-01  BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P /	155157-01  BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P /	155151-01  BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P /	155152-01  BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P /	155153-01  BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P /	155154-01  BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P /	155155-01  BD PYXIS MEDBANK TWR MN CR-2HH-6FH /	155146-01  BD PYXIS MEDBANK TWR MN CR-2HH-6FM /	155147-01  BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P /	155148-01  BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P /	155149-01  BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P /	155150-01  BD PYXIS ME

## Reason for recall

Due to a software issue, when attempting to restock the automated dispensing cabinet, user have received the banner message "Stocking window has passed, or item has been removed from purchase order. Please contact Pharmacy for assistance".  When this occurs, the medication cannot be restocked and can potentially lead to delays in accessing medication for patients.

## Distribution

U.S.: AL,AZ, CA, CT, FL, GA, IA, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NY, OH, PA, TN, TX, UT, VA, WA, WI and WV.  O.U.S.: None

## Key facts

- **Recall number:** Z-1550-2025
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-11
- **Report date:** 2025-04-16

- **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-1550-2025

## Citation

> AI Analytics. FDA recall Z-1550-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1550-2025. Source: US FDA. Licensed CC0.

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