# FDA recall Z-2321-2025

> **CareFusion 303, Inc.** · Class III · device recall initiated 2025-07-10.

## Product

Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137,		 BD PYXIS MEDBANK MINI 4HM/169-113,		 BD PYXIS MEDBANK MINI 4HH/169-112,		 BD PYXIS MEDBANK MINI 3HH-1HM/169-111,		 BD PYXIS MEDBANK MINI 3HH-1FG/169-110,	 BD PYXIS MEDBANK MINI 2HM-1FM/169-109,		 BD PYXIS MEDBANK MINI 2HH-2HM/169-108,		 BD PYXIS MEDBANK MINI 2HH-1FM/169-107,	 BD PYXIS MEDBANK MINI 2HH-1FH/169-106,		 BD PYXIS MEDBANK MINI 2FM/169-105,		 BD PYXIS MEDBANK MINI 2FH/169-104,		 BD PYXIS MEDBANK MINI 1HH-3HM/169-103,		 BD PYXIS MEDBANK MINI 1HH-1HM-1FM/169-102,		 BD PYXIS MEDBANK MINI 1HH-1FH-1HM/169-101	,	 BD PYXIS MEDBANK MINI 1FH-2HH/155311-01,		 BD PYXIS MEDBANK MINI 4HH/155310-01,		 BD PYXIS MEDBANK MINI 1FH-1FM/155288-01,		 BD PYXIS MEDBANK MINI 4HM/155171-01,		 BD PYXIS MEDBANK MINI 3HH-1HM/155169-01,		 BD PYXIS MEDBANK MINI 3HH-1FG/155168-01,		 BD PYXIS MEDBANK MINI 2HM-1FM/155167-01,		 BD PYXIS MEDBANK MINI 2HH-2HM/155166-01,		 BD PYXIS MEDBANK MINI 2HH-1FM/155165-01,		 BD PYXIS MEDBANK MINI 2FM/155163-01,		 B

## Reason for recall

Reports of delayed access to medication in automated dispensing cabinets because of the override/Add Item workflow.

## Distribution

US Nationwide distribution including in the states of NY, MA, KY, VA, OR, OH, FL, WA, MS, OK, TN, PA, RI, TX, SC, AR, MI, NJ, CT, MD, AZ, CA, WV, NC, UT, WY, CO, SD, ID, IL, IN, NV, NM, NE, KS, GA, WI, MO, IA, ME, LA, MN, AL, VT, NH, DE, MT, ND, AK, HI, DC.

## Key facts

- **Recall number:** Z-2321-2025
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-10
- **Report date:** 2025-08-20

- **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-2321-2025

## Citation

> AI Analytics. FDA recall Z-2321-2025. Retrieved 2026-09-16 from https://api.ai-analytics.org/recall/Z-2321-2025. Source: US FDA. Licensed CC0.

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