Quick Facts at a Glance
- Recall Date
- April 10, 2025
- Hazard Level
- HIGH
- Brand
- 3M
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- 3M
- Product type
- Blood/Fluid Warming High Flow Set
- Model numbers
- 24355, 24370
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
April 10, 2025
Reported by FDA DEVICE
September 24, 2025
RecallRadar source check
April 18, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact 3M Company or your healthcare provider for instructions. Notification method: Letter
About This Product
The 3M Ranger Blood/Fluid Warming High Flow Sets are designed to warm blood and fluids before administering them to patients, ensuring that fluids are at a safe temperature for infusion. Medical professionals typically use these devices during surgeries or in emergency situations.
Why This Is Dangerous
Incorrect flow rates and temperatures can lead to potentially unsafe infusion of fluids. If fluids are not warmed adequately, patients may experience hypothermia during a critical medical procedure.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall impacts a significant number of devices used daily in healthcare settings, emphasizing the need for accurate monitoring of blood and fluid temperatures during medical treatments.
Practical Guidance
How to identify if yours is affected
- Check catalog number on your device for 24355 or 24370
- Confirm the device is not in use
- Review packaging or device labeling for any recall notices
Where to find product info
Catalog numbers can typically be located on the product packaging, device labels, or user manuals.
What timeline to expect
Expect a timeline of 4-6 weeks for refund processing after the manufacturer has received the returned device.
If the manufacturer is unresponsive
- Contact customer service again; provide documentation of your recall requests.
- Reach out to the FDA or relevant health authorities if issues persist.
How to prevent similar issues
- Always verify device information and manuals before use.
- Stay updated on manufacturer recalls and safety notices.
- Ensure proper training for all staff using medical devices.
Documentation advice
Keep copies of receipts, recall correspondence, and any communication with 3M regarding the return process.
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Product Details
Catalog Numbers: 24355, 24370 Global Distribution: US, Canada, Europe, Asia, and Australia Quantity: 530,470 units
Reported Incidents
No injuries or incidents have been reported.
Key Facts
- Hazard: Incorrect flow rates and outlet temperature
- Global distribution includes multiple countries
- Stop using immediately and follow recall instructions
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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