FDA Device recall Z-2110-2021
Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled administration of fluids
- FDA Device
- Class I
- terminated
- Published 2021-08-18
On 2021-08-18 the FDA classified a Class I recall of Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled administration of fluids by Baxter Healthcare, citing system errors were noted following changes the customers implemented to the configuration of their network and server systems. Gateway Server System performance anomalies resulted….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2110-2021 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2021-06-04 |
| Published | 2021-08-18 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | PR |
Product
Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled administration of fluids.
Reason
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.
Identifiers
| code_info | All Serial Numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2110-2021%22
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