# FDA recall Z-1002-2024

> **Baxter Healthcare Corporation** · Class I · device recall initiated 2023-12-22.

## Product

Baxter Exactamix Pro 2400, REF EXM24DY

## Reason for recall

An error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in redundant ingredient delivery of the requested overfill volume.

## Distribution

US:  AL, AZ, CA, FL, GA, IA, KY, MD, MI, MN, MO, NC, NE, NH, NJ, NV, NY, OR, SD, TX, WA, WI,

## Key facts

- **Recall number:** Z-1002-2024
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-22
- **Report date:** 2024-02-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1002-2024

## Citation

> AI Analytics. FDA recall Z-1002-2024. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/Z-1002-2024. Source: US FDA. Licensed CC0.

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