Dose IQ Safety Software used with Spectrum IQ Infusion Pump
Reported: August 18, 2021 Initiated: July 7, 2021 #Z-2165-2021
Product Description
Dose IQ Safety Software used with Spectrum IQ Infusion Pump
Reason for Recall
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.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 61 units
- Distribution
- US Nationwide Distribution.
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Dose IQ Safety Software used with Spectrum IQ Infusion Pump. Recalled by Baxter Healthcare Corporation. Units affected: 61 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 18, 2021. Severity: Critical. Recall number: Z-2165-2021.
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