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.
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.
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
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 recall stems from the need to clarify flow rates and fluid temperatures. Misunderstandings in these areas pose a high risk to patient safety.
No specific incidents or injuries have been reported related to this recall. The classification is deemed Class I, indicating a high hazard.
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.
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.
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