# FDA recall Z-2415-2025

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2025-07-14.

## Product

Spectrum IQ Infusion Pump, Product Code 3570009

## Reason for recall

Baxter has identified that certain pumps have potentially been released with the grease applied to the cam and motor gears that will break down quickly. The breakdown of the grease will lead to the device having insufficient or ineffective grease applied to the cam, which could lead to premature wear of the mechanism assembly, resulting in excessive therapy.

## Distribution

US distribution to states of: AZ, FL

## Key facts

- **Recall number:** Z-2415-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-14
- **Report date:** 2025-09-03

- **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-2415-2025

## Citation

> AI Analytics. FDA recall Z-2415-2025. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-2415-2025. Source: US FDA. Licensed CC0.

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