# FDA recall Z-1423-2025

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2025-03-03.

## Product

Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS

## Reason for recall

Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed below due to an incorrectly installed gasket. A gasket failure could lead to potential fluid ingress due to cleaning, or as a result of an IV fluid spill.

## Distribution

US Nationwide distribution in the states of AR, CA, FL, IA, IN, LA, MO, MT, NC, NY, OH, OR, PA, TN, TX, VA, WA, WI, WV.

## Key facts

- **Recall number:** Z-1423-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-03
- **Report date:** 2025-04-02

- **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-1423-2025

## Citation

> AI Analytics. FDA recall Z-1423-2025. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1423-2025. Source: US FDA. Licensed CC0.

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