Drug recall
3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370
FDA recall event 96841 · Class I · 3M Company
Key facts
| Event ID | 96841 |
|---|---|
| Recall numbers | Z-2483-2025 |
| Recalling firm | 3M Company |
| Product type | Devices |
| Products | 3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370 |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Field action to clarify the flow rates and inlet fluid temperatures, along with location of the outlet temperature for Ranger Blood/Fluid Warming High Flow Sets. |
| Initiation date | Apr 10, 2025 |
| Report date | Sep 24, 2025 |
| City | Saint Paul |
| State | MN |
| Country | United States |
| FEI number | 2110898 |
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: