Baxter Healthcare Corporation recalls Spectrum IQ Infusion Pump, Product Code 3570009

Recall date

July 14, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2415-2025

FDA classification

Class II

Brand / firm

Baxter Healthcare Corporation

Sold / distributed

US distribution to states of: AZ, FL

Why it was recalled

Baxter has identified that certain pumps have potentially been released with the grease applied to the cam and motor gears that will break down quickly. The breakdown of the grease will lead to the device having insufficient or ineffective grease applied to the cam, which could lead to premature wear of the mechanism assembly, resulting in excessive therapy.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Spectrum IQ Infusion Pump, Product Code 3570009