Recall
FDAHealthJuly 14, 2025

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

⚠️ 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.

Is this relevant to me?

Geography
US, AZ, FL
Source agency
FDA
Category
Health
Published
July 14, 2025

US distribution to states of: AZ, FL

What's affected?

Product
Spectrum IQ Infusion Pump, Product Code 3570009
Lot code
UDI-DI: 00085412610900; Serial Numbers: 3815255 3815261 3815265 3815266 3815267 3815271

Additional details

UDI-DI: 00085412610900; Serial Numbers: 3815255 3815261 3815265 3815266 3815267 3815271

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 6 units.

View original FDA notice →

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