# FDA recall Z-0529-2022

> **Baxter Healthcare Corporation** · Class I · device recall initiated 2021-12-29.

## Product

Baxter Spectrum IQ Infusion Pumps, Product code 3570009.

## Reason for recall

There is the potential for reduced or non-delivery of medication, in some cases without alerting the user via pump alarm. This may occur as a result of incorrect administration set setup and/or incomplete resolution of upstream occlusion alarms when using Spectrum V8 and Spectrum IQ infusion pumps.

## Distribution

Worldwide Distribution.  US nationwide Puerto Rico and St. Thomas.  There was government/military distribution.  Countries of Canada, Bahamas, Barbados, Bermuda, Guyana, Jamaica, and Trinidad and Tobago.

## Key facts

- **Recall number:** Z-0529-2022
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-12-29
- **Report date:** 2022-02-09

- **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-0529-2022

## Citation

> AI Analytics. FDA recall Z-0529-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0529-2022. Source: US FDA. Licensed CC0.

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