# FDA recall Z-2948-2024

> **CareFusion 303, Inc.** · Class II · device recall initiated 2024-07-09.

## Product

BKIT BD Pyxis QFill Replenishment Station, REF: 155197-01, medication cabinet system

## Reason for recall

Due to software issue, there is a potential when a restock label is printed for a medication stored in a non-CUBIE location, that the incorrect bin for the medication is printed on the label.

## Distribution

US Nationwide distribution in the states of CA, FL, KS, MN, NJ, NY, PA.

## Key facts

- **Recall number:** Z-2948-2024
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-09
- **Report date:** 2024-09-11

- **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-2948-2024

## Citation

> AI Analytics. FDA recall Z-2948-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2948-2024. Source: US FDA. Licensed CC0.

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