Medical device recalls High risk

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

Recall date
April 10, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2483-2025
FDA classification
Class I
Brand / firm
3M Company
Sold / distributed
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,…

Why it was recalled

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.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

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

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