# FDA recall Z-2582-2024

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

## Product

Spectrum Wireless Battery Modules A/B/G/N, product code 36010, used with either of the following 35700BAX2 (Spectrum V8 infusion pump) and 3570009 (Spectrum IQ 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-2582-2024
- **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-2582-2024

## Citation

> AI Analytics. FDA recall Z-2582-2024. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-2582-2024. Source: US FDA. Licensed CC0.

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