PlainRecalls
FDA Devices Moderate Class II Ongoing

Spectrum IQ Infusion Pump, Product Code 3570009

Reported: September 3, 2025 Initiated: July 14, 2025 #Z-2415-2025

Product Description

Spectrum IQ Infusion Pump, Product Code 3570009

Reason for Recall

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.

Details

Units Affected
6 units
Distribution
US distribution to states of: AZ, FL
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
Spectrum IQ Infusion Pump, Product Code 3570009. Recalled by Baxter Healthcare Corporation. Units affected: 6 units.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 3, 2025. Severity: Moderate. Recall number: Z-2415-2025.