Baxter Healthcare Corporation Recall 88246
Description: Dose IQ Safety Software used with Spectrum IQ Infusion Pump
Baxter Healthcare Corporation Recall 88246 Information
Status | Ongoing |
Mandated? | Voluntary: Firm initiated |
Recall Number | Z-2165-2021 |
Event ID | 88246 |
Event Description | Dose IQ Safety Software used with Spectrum IQ Infusion Pump |
Product Type | Devices |
Distribution | US Nationwide Distribution. |
Quantity | 61 units |
Recall Reason | 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. |
Device Classification | 20210818 |
Device Code Info | Software version: All libraries initially created with version 9.0.x |
Center Classification Date | 20210811 |
Recall Initiation Date | 20210707 |
Recalling Firm | Baxter Healthcare Corporation |
Initial Notification | Letter |
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