# FDA recall Z-2483-2025

> **3M Company** · Class I · device recall initiated 2025-04-10.

## Product

3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370

## 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.

## Distribution

Worldwide distribution. US nationwide including Puerto Rico, Argentina, Australia, Austria, Belgium, Bosnia and Herzegovina, Canada, Canary Islands, China, Costa Rica, Croatia, Czechia, Denmark, Estonia, Finland, France, French Guiana, French Polynesia, Germany, Greece, Hong Kong, Hungary, Ireland, Israel, Italy, Jordan, Korea, Luxembourg, Netherlands, New Caledonia, New Zealand, Norway, Poland, Portugal, Qatar, Reunion, Romania, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, Spain, Sweden, Switzerland, Taiwan, Thailand, UAE, UK, and Vietnam.

## Key facts

- **Recall number:** Z-2483-2025
- **Recalling firm:** 3M Company
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-10
- **Report date:** 2025-09-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Paul, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2483-2025

## Citation

> AI Analytics. FDA recall Z-2483-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2483-2025. Source: US FDA. Licensed CC0.

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