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 recordK-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.