# FDA recall Z-2581-2024

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2024-07-17.

## Product

Baxter Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with either of the following:  35700BAX2 (Spectrum V8 infusion pump) or 3570009 (Spectrum IQ infusion pump) Baxter SIGMA Spectrum V8 Infusion Pump

## Reason for recall

The Spectrum WBM may fail to auto-document infusion status information back to the hospital's Electronic Medical Record (EMR) system. This software issue only impacts customers where the Spectrum V8 or Spectrum IQ infusion system is integrated with the hospital s EMR system.

## Distribution

US, Nationwide

## Key facts

- **Recall number:** Z-2581-2024
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-17
- **Report date:** 2024-08-28

- **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-2581-2024

## Citation

> AI Analytics. FDA recall Z-2581-2024. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-2581-2024. Source: US FDA. Licensed CC0.

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