# FDA recall Z-2165-2021

> **Baxter Healthcare Corporation** · Class I · device recall initiated 2021-07-07.

## Product

Dose IQ Safety Software used with Spectrum IQ Infusion Pump

## Reason for recall

Software issue:  The defect creates a mismatch between linked drug identifiers (IDs) in the Dose IQ user interface (UI) and the binary drug library (BDL) loaded onto the Spectrum IQ pump.

## Distribution

US Nationwide Distribution.

## Key facts

- **Recall number:** Z-2165-2021
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-07-07
- **Report date:** 2021-08-18
- **Termination date:** 2024-06-20

- **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-2165-2021

## Citation

> AI Analytics. FDA recall Z-2165-2021. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-2165-2021. Source: US FDA. Licensed CC0.

---

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