# FDA recall Z-1785-2022

> **CareFusion 303, Inc.** · Class II · device recall initiated 2022-05-24.

## Product

BD Pyxis MedBank Cabinet Software v2.1.2.9      Legacy MedBank Cabinets with Matrix Drawers include:  .	CUBEX MedFlex operating with Windows 7   .	MedBank 200 Main operating with Windows 7  . 	MedBank 500 Main operating with Windows 7.      An automated dispensing cabinet intended to securely store and dispense medications to health care providers in a clinical setting.

## Reason for recall

The automated dispensing cabinet software update included a .dll file that is not compatible with MedBank Cabinet stations with MedCart Matrix drawers.  The cabinet system will stop functioning (Matrix drawers will stop opening in the MedBank Application) leading to delay in access to medications or supplies needed in residential or procedural care facilities.

## Distribution

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

## Key facts

- **Recall number:** Z-1785-2022
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-05-24
- **Report date:** 2022-10-05

- **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-1785-2022

## Citation

> AI Analytics. FDA recall Z-1785-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1785-2022. Source: US FDA. Licensed CC0.

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