Drug recall
Spectrum IQ Infusion Pump, Product Code 3570009
FDA recall event 97335 · Class II · Baxter Healthcare Corporation
Key facts
| Event ID | 97335 |
|---|---|
| Recall numbers | Z-2415-2025 |
| Recalling firm | Baxter Healthcare Corporation |
| Product type | Devices |
| Products | Spectrum IQ Infusion Pump, Product Code 3570009 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Baxter has identified that certain pumps have potentially been released with the grease applied to the cam and motor gears that will break down quickly. The breakdown of the grease will lead to the… |
| Initiation date | Jul 14, 2025 |
| Report date | Sep 3, 2025 |
| 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: