PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: November 20, 2024 Initiated: October 2, 2024 #Z-0348-2025

Product Description

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

Reason for Recall

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

Details

Units Affected
8 units
Distribution
GA, ID
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. Recalled by Baxter Healthcare Corporation. Units affected: 8 units.
Why was this product recalled?
The door on the Spectrum IQ Infusion pump may not be able to fully close.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 20, 2024. Severity: Moderate. Recall number: Z-0348-2025.