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Baxter Healthcare Corporation recalls Dose IQ Safety Software used with Spectrum IQ Infusion Pump
Recalled August 18, 2021 · FDA recall Z-2165-2021 · Baxter Healthcare
Hazard
Software issue: The defect creates a mismatch between linked drug identifiers (IDs) in the Dose IQ user interface (UI) and the binary drug library (BDL) loaded onto the Spectrum IQ pump. · FDA Class I
Units
61 units
Sold at
US Nationwide Distribution.
Description
Software issue: The defect creates a mismatch between linked drug identifiers (IDs) in the Dose IQ user interface (UI) and the binary drug library (BDL) loaded onto the Spectrum IQ pump.
Product
Dose IQ Safety Software used with Spectrum IQ Infusion Pump
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →