Baxter Healthcare Corporation: Medical Device Recall in 2024 - (Recall #: Z-0348-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009

Product Classification:

Class II

Date Initiated: October 2, 2024

Date Posted: November 20, 2024

Recall Number: Z-0348-2025

Event ID: 95505

Reason for Recall:

The door on the Spectrum IQ Infusion pump may not be able to fully close.

Status: Ongoing

Product Quantity: 8 units

Code Information:

00085412610900, Serial Numbers: 3796578, 3797382, 3797464, 3797578, 3797728, 3797733, 3798019, 3798200

Distribution Pattern:

GA, ID

Voluntary or Mandated:

Voluntary: Firm initiated