3M Company: Device Recall

Recall #Z-2483-2025 · 04/10/2025

Class I: Dangerous

Recall Details

Recall Number: Z-2483-2025
Classification: Class I
Product Type: Device
Recalling Firm: 3M Company
Status: Ongoing
Date Initiated: 04/10/2025
Location: Saint Paul, MN, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 530,470 units

Reason for Recall

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.

Product Description

3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370

Distribution Pattern

Worldwide distribution. US nationwide including Puerto Rico, Argentina, Australia, Austria, Belgium, Bosnia and Herzegovina, Canada, Canary Islands, China, Costa Rica, Croatia, Czechia, Denmark, Estonia, Finland, France, French Guiana, French Polynesia, Germany, Greece, Hong Kong, Hungary, Ireland, Israel, Italy, Jordan, Korea, Luxembourg, Netherlands, New Caledonia, New Zealand, Norway, Poland, Portugal, Qatar, Reunion, Romania, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, Spain, Sweden, Switzerland, Taiwan, Thailand, UAE, UK, and Vietnam.

Other Recalls by 3M Company

Class II: Risk 04/22/2025

Notice was issued to clarify flow rates related to the inlet fluid temperature.

View all recalls by 3M Company →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.