3M Ranger Blood/Fluid Warming High Flow Sets Recalled to Clarify Safety

Agency Publication Date: September 18, 2025

Summary

3M Company has initiated a voluntary recall of approximately 530,470 Ranger Blood/Fluid Warming High Flow Sets, catalog numbers 24355 and 24370, manufactured after March 2022. This action is being taken to provide essential clarifications for safety instructions regarding fluid flow rates, inlet temperatures, and the specific location where outlet temperature is measured. There have been no reported incidents or injuries associated with this clarification update.

Risk

Unclear safety instructions regarding flow rates and temperatures can lead to improper fluid warming management during medical procedures. While no injuries have been reported, accurate operating parameters are critical for ensuring the device performs safely and effectively for patients.

What You Should Do

This recall affects 3M Ranger Blood/Fluid Warming High Flow Sets with catalog numbers 24355 and 24370 that were manufactured at any time after March 2022.
Identify if your facility has these products by checking the catalog number and the manufacturing date printed on the individual product packaging or shipping cartons.
Stop using the recalled devices according to existing instructions. Contact 3M Company or your medical distributor to obtain the updated safety instructions and clarified flow rate guidelines.
Facilities should ensure that all clinical staff who use these warming sets are briefed on the corrected instructions once they are received from the manufacturer.
Contact 3M Company directly for any further guidance regarding the return, replacement, or correction of these sets.
Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls if you have additional questions regarding this medical device recall.

Your Remedy Options

Other Action

How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: 3M Ranger Blood/Fluid Warming High Flow Set

Model / REF:

24355

24370

Date Ranges: Manufactured after March 2022

Recall Number: Z-2483-2025; Total affected quantity: 530,470 units.

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 96841

Status: Active

Manufacturer: 3M Company

Sold By: Medical distributors; Direct healthcare facility sales

Manufactured In: United States

Units Affected: 530,470 units

Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.

Summary

What You Should Do

This recall affects 3M Ranger Blood/Fluid Warming High Flow Sets with catalog numbers 24355 and 24370 that were manufactured at any time after March 2022.

Identify if your facility has these products by checking the catalog number and the manufacturing date printed on the individual product packaging or shipping cartons.

Stop using the recalled devices according to existing instructions. Contact 3M Company or your medical distributor to obtain the updated safety instructions and clarified flow rate guidelines.

Facilities should ensure that all clinical staff who use these warming sets are briefed on the corrected instructions once they are received from the manufacturer.

Contact 3M Company directly for any further guidance regarding the return, replacement, or correction of these sets.

Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls if you have additional questions regarding this medical device recall.