# FDA recall Z-1368-2026

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2026-01-13.

## Product

Brand Name: Spectrum IQ  Product Name: Infusion Pump  Model/Catalog Number: 3570009  Software Version: N/A  Product Description: Infusion Pump, one unit per carton  Component: N/A

## Reason for recall

Pumps were released without full testing being performed, including occlusion alarm testing.

## Distribution

States: Ohio  Countries: United States

## Key facts

- **Recall number:** Z-1368-2026
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-13
- **Report date:** 2026-02-25

- **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-1368-2026

## Citation

> AI Analytics. FDA recall Z-1368-2026. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-1368-2026. Source: US FDA. Licensed CC0.

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