# FDA recall Z-0151-2024

> **Baxter Healthcare Corporation** · Class I · device recall initiated 2023-10-13.

## Product

Novum IQ Syringe infusion system, Product Code 40800BAXUS

## Reason for recall

Baxter is issuing an Urgent Medical Device Correction for the Novum IQ Syringe Pump. Baxter identified that after multiple downstream occlusion alarms, the pump may display an  Infusion Complete  alarm even though uninfused fluid remains in the syringe.

## Distribution

US Nationwide Distribution to states of: AR, AZ, CA, FL, GA, HI, IA, IN, KS, LA, MD, MI, MN, MO, NC, NE, NH, NJ, NY, PA, TX, UT, VA, VT, WA, WI AND WV.

## Key facts

- **Recall number:** Z-0151-2024
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-10-13
- **Report date:** 2023-11-15

- **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-0151-2024

## Citation

> AI Analytics. FDA recall Z-0151-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0151-2024. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*