HIGH

3M Recalls Ranger Blood/Fluid Warming Sets Over Flow Rate Issues

3M recalled 530,470 Ranger Blood/Fluid Warming High Flow Sets on April 10, 2025. The recall addresses concerns about flow rates and inlet temperatures. Healthcare providers and patients must stop using the devices immediately.

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

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

Product Details

The recall includes Ranger Blood/Fluid Warming High Flow Sets with catalog numbers 24355 and 24370. These products were distributed worldwide, including the US and Puerto Rico, from March 2022 onwards.

The Hazard

The recall stems from the need to clarify flow rates and fluid temperatures. Misunderstandings in these areas pose a high risk to patient safety.

Reported Incidents

No specific incidents or injuries have been reported related to this recall. The classification is deemed Class I, indicating a high hazard.

What to Do

Patients and healthcare providers should stop using the devices immediately. Follow the recall instructions provided by 3M and contact your healthcare provider for further guidance.

Contact Information

For more information, contact 3M Company or visit the FDA recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-2483-2025.

Key Facts

  • 530,470 units recalled
  • Catalog Numbers: 24355, 24370
  • Class I recall due to high hazard
  • Worldwide distribution including US and Puerto Rico

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeBlood/Fluid Warming Set
Sold At
Multiple Retailers

Product Details

Brand
Model Numbers
24355
24370
Affected States
ALL
Report Date
September 24, 2025
Source Agency
FDA - Medical Devices
Recall Status
ACTIVE

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