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 |
| Similar To |