# FDA recall Z-1207-2025

> **CareFusion 303, Inc.** · Class II · device recall initiated 2025-01-23.

## Product

BD Pyxis MedFlex 2.0 REF 1139-00    Bio-ID Spare Parts REF 353200-01    The BD Pyxis" MedFlex is an Automated Dispensing Cabinet (ADC) intended to securely store and dispense medications and supplies to a qualified and authorized user in a clinical setting.

## Reason for recall

Due to fingerprint scanner failing resulting in the scanner heating up.

## Distribution

Worldwide - U.S. Nationwide distribution including in the states of AL, AZ, CA, CO, CT, DC, DE, FL, GA, Guam, HI , IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, VA, VT, WA, WI, and WY. The countries of Australia, Bahrain, Belgium, Brazil, Canada, Hong Kong, Kuwait, Lebanon, New Zealand, Qatar, Saudi Arabia, Spain, and Thailand.

## Key facts

- **Recall number:** Z-1207-2025
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-01-23
- **Report date:** 2025-03-05

- **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-1207-2025

## Citation

> AI Analytics. FDA recall Z-1207-2025. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-1207-2025. Source: US FDA. Licensed CC0.

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