Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2110-2021 — Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled administration of fluids.

U.S. FDA — Device Enforcement · United States · 2021-06-04 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2110-2021
Date of alert
2021-06-04
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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