Recall Z-2483-2025— 3M Company

Name: FDA recall Z-2483-2025
Creator: U.S. Food and Drug Administration
Published: 2025-04-10

Class I · Ongoing

Class I FDA medical device recall by 3M Company, initiated 2025-04-10. It names one FDA 510(k) clearance: K973741. Product: 3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370. Reason: 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..

Recalling firm: 3M Company
Classification: Class I
Status: Ongoing
Initiated: 2025-04-10
Firm location: Saint Paul, MN, United States

510(k) clearances named in this recall

1 on FDA's record

K973741 — BAIR HUGGER BLOOD/FLUID WARMERAugustine Medical, Inc.·cleared 1998-04-30

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

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

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.