Recall Z-2231-2025— 3M Company

Class II · Ongoing

Class II FDA medical device recall by 3M Company, initiated 2025-04-22. It names one FDA 510(k) clearance: K060939. Product: 3M Ranger Irrigation Fluid Warming Set, REF 24750. Reason: Notice was issued to clarify flow rates related to the inlet fluid temperature..

Recalling firm
3M Company
Classification
Class II
Status
Ongoing
Initiated
2025-04-22
Firm location
Saint Paul, MN, United States

510(k) clearances named in this recall

1 on FDA's record

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 Irrigation Fluid Warming Set, REF 24750

Reason for recall

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

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