---
title: "3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370 — FDA record Z-2483-2025 | Is It on Recall"
description: "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"
url: https://isitonrecall.com/recall/fda-device-z-2483-2025-3m-ranger-blood-fluid-warming-high-flow-set-catalog-numbers-24355-24370/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# 3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370 — FDA record Z-2483-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 10, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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.
- **Classification**: Class I
- **Recalling firm**: 3M Company
- **Quantity**: 530,470 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2483-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2483-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | All lots with a manufacturing date after March 2022. |

Match all identifying details in the current notice. A brand name alone is not enough.

## 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.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Sep 24, 2025
- **Recall initiation date**: Apr 10, 2025
- **Center classification date**: Sep 18, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2483-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [3M Company records](https://isitonrecall.com/brand/3m-company/)
