# FDA recall Z-0962-2026

> **CareFusion 303, Inc.** · Class II · device recall initiated 2025-11-20.

## Product

BD Pyxis MedStation ES, REF: 323,    BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324,   BD Pyxis MedStation ES Tower, REF: 352,   BD Pyxis Pro 7-Drawer Auxiliary, REF: 1149-00,   BD Pyxis Pro 7- Drawer Auxiliary with Secure Tower, REF: 1152-00,   BD Pyxis Pro MedStation Main, REF: 1155-00,    BD Pyxis CII Safe ES, REF: 1116-00

## Reason for recall

Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a duplicate address, which causes an error and the drawer to fail, which may lead to inability or delay in accessing stored items, delay in the replenishment of ADCs or patient specific medications stored outside of ADCs.

## Distribution

Worldwide - US Nationwide distribution including in the states of  CO, IN, OH, TX, KS, FL, GA, NC, CA, HI, IL, NY, MI, VA, AL, LA, NE, KY, OK, AR, TN, WY, NJ, WI, SD, AZ, NV, MO, MA, ID, WV, DE, PA, WA, MT, CT, IA, MD, PR, MN, NM, OR, VT, MS, ME, AK, UT, DC, GU, SC, NH, RI, ND, AS and the countries of CH, CA, KW, QA, NL, GB, UY, AU, NZ, BH, TH, SG, CN, FR, LB, BS, HK, TR, PL, AR, BR, CL, CO, MX, ES, BM, SA, IL.

## Key facts

- **Recall number:** Z-0962-2026
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-11-20
- **Report date:** 2025-12-31

- **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-0962-2026

## Citation

> AI Analytics. FDA recall Z-0962-2026. Retrieved 2026-09-04 from https://api.ai-analytics.org/recall/Z-0962-2026. Source: US FDA. Licensed CC0.

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