FDA Device recall Z-2483-2025
3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370
- FDA Device
- Class I
- ongoing
- Published 2025-09-24
On 2025-09-24 the FDA classified a Class I recall of 3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370 by 3m, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2483-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-04-10 |
| Published | 2025-09-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | 3m |
| Distribution | US |
Product
3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370
Reason
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.
Identifiers
| code_info | All lots with a manufacturing date after March 2022. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2483-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.