Drug recall
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
FDA recall event 95505 · Class II · Baxter Healthcare Corporation
Key facts
| Event ID | 95505 |
|---|---|
| Recall numbers | Z-0348-2025 |
| Recalling firm | Baxter Healthcare Corporation |
| Product type | Devices |
| Products | Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The door on the Spectrum IQ Infusion pump may not be able to fully close. |
| Initiation date | Oct 2, 2024 |
| Report date | Nov 20, 2024 |
| City | Deerfield |
| State | IL |
| Country | United States |
| FEI number | 1417572 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: