# FDA recall Z-1767-2025

> **Baxter Healthcare Corporation** · Class I · device recall initiated 2025-04-24.

## Product

Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS

## Reason for recall

There is a potential for the Novum IQ LVP due to the potential for underinfusion following use of the "standby mode" feature or if the device is powered off with the set loaded.

## Distribution

US and Canada

## Key facts

- **Recall number:** Z-1767-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-24
- **Report date:** 2025-05-28

- **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-1767-2025

## Citation

> AI Analytics. FDA recall Z-1767-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1767-2025. Source: US FDA. Licensed CC0.

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