Baxter Healthcare Corporation: Medical Device Recall in 2021 - (Recall #: Z-2110-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled administration of fluids.

Product Classification:

Class I

Date Initiated: June 4, 2021

Date Posted: August 18, 2021

Recall Number: Z-2110-2021

Event ID: 88073

Reason for Recall:

System errors were noted following changes the customers implemented to the configuration of their network and server systems. Gateway Server System performance anomalies resulted in excessive Spectrum IQ pump connectivity errors.

Status: Terminated

Product Quantity: 130135 units

Code Information:

All Serial Numbers

Distribution Pattern:

United States (including Puerto Rico), Canada, Bahamas, Bermuda, Guyana, and Trinidad and Tobago.

Voluntary or Mandated:

Voluntary: Firm initiated