Baxter Healthcare Corporation: Medical Device Recall in 2025 - (Recall #: Z-2415-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Spectrum IQ Infusion Pump, Product Code 3570009

Product Classification:

Class II

Date Initiated: July 14, 2025

Date Posted: September 3, 2025

Recall Number: Z-2415-2025

Event ID: 97335

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.

Status: Ongoing

Product Quantity: 6 units

Code Information:

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

Distribution Pattern:

US distribution to states of: AZ, FL

Voluntary or Mandated:

Voluntary: Firm initiated