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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

3M Ranger Irrigation Fluid Warming Sets Recalled for Flow Rate Clarification

Agency Publication Date: August 1, 2025
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Summary

3M Company is recalling approximately 186,880 units of the 3M Ranger Irrigation Fluid Warming Set (Model 24750). The recall was issued to provide essential clarification on how flow rates are affected by the temperature of the fluid entering the device. No injuries or incidents have been reported, but the update ensures medical staff have accurate performance data during procedures.

Risk

If the flow rate is not correctly understood in relation to fluid temperature, medical professionals might not achieve the intended warming levels during irrigation. This could potentially affect patient temperature management during clinical procedures.

What You Should Do

  1. This recall affects 3M Ranger Irrigation Fluid Warming Sets, Model REF 24750, manufactured after March 2022.
  2. Identify the affected products by checking the box or pouch for Model REF 24750, SKU 7100235070, or UDI numbers 50707387792720 and 10707387792722.
  3. Confirm if the manufacturing date on your specific units is after March 2022.
  4. Stop using the recalled device immediately.
  5. Contact 3M Company or your medical distributor to arrange for a return, replacement, or to receive updated documentation regarding the flow rate clarifications.
  6. Call the FDA at 1-888-463-6332 if you have additional questions regarding this medical device recall.

Your Remedy Options

๐Ÿ“‹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 Irrigation Fluid Warming Set
Model / REF:
24750
UDI:
50707387792720
10707387792722
Date Ranges: Manufactured after March 2022

SKU 7100235070; All lots with a manufacturing date after March 2022 are affected.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97174
Status: Active
Manufacturer: 3M Company
Sold By: Medical distributors; Direct hospital sales
Manufactured In: United States
Units Affected: 186,880 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 ยท 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.