Baxter Healthcare Corporation recalls Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
- Recall date
- October 2, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0348-2025
- FDA classification
- Class II
- Brand / firm
- Baxter Healthcare Corporation
- Sold / distributed
- GA, ID
Why it was recalled
The door on the Spectrum IQ Infusion pump may not be able to fully close.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
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