# FDA recall Z-2332-2025

> **Baxter Healthcare Corporation** · Class I · device recall initiated 2025-08-04.

## Product

Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump

## Reason for recall

Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only).

## Distribution

US distribution including Puerto Rico and OUS (International) Canada

## Key facts

- **Recall number:** Z-2332-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-04
- **Report date:** 2025-09-10

- **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-2332-2025

## Citation

> AI Analytics. FDA recall Z-2332-2025. Retrieved 2026-07-25 from https://api.ai-analytics.org/recall/Z-2332-2025. Source: US FDA. Licensed CC0.

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