# FDA recall Z-1487-2021

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2021-03-19.

## Product

Spectrum IQ - Infusion Pump - Product Usage: intended to be used for the controlled administration of fluids.

## Reason for recall

Potentially defective component in the AC power adapter which may fail over time.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AL, AR, CA, CT, FL, IA, IN, LA, MA, MD, ME, MN, MO, MS, MT, NC, NJ, NY, OH, PA, RI, SC, TN, TX and the country of  Puerto Rico.

## Key facts

- **Recall number:** Z-1487-2021
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-03-19
- **Report date:** 2021-05-05
- **Termination date:** 2022-07-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Medina, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1487-2021

## Citation

> AI Analytics. FDA recall Z-1487-2021. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/Z-1487-2021. Source: US FDA. Licensed CC0.

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