# FDA recall Z-2110-2021

> **Baxter Healthcare Corporation** · Class I · device recall initiated 2021-06-04.

## Product

Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009.  for the controlled administration of fluids.

## Reason for recall

System errors were noted following changes the customers implemented to the configuration of their network and server systems. Gateway Server System performance anomalies resulted in excessive Spectrum IQ pump connectivity errors.

## Distribution

United States (including Puerto Rico), Canada, Bahamas, Bermuda, Guyana, and Trinidad and Tobago.

## Key facts

- **Recall number:** Z-2110-2021
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-06-04
- **Report date:** 2021-08-18
- **Termination date:** 2024-09-25

- **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-2110-2021

## Citation

> AI Analytics. FDA recall Z-2110-2021. Retrieved 2026-09-08 from https://api.ai-analytics.org/recall/Z-2110-2021. Source: US FDA. Licensed CC0.

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