FDA Medical devices recall ·

3M Ranger Irrigation Fluid Warming Set recall

Recall number
Z-2231-2025
Date
(initiated April 22, 2025)
Company / brand
3M Company
2510 Conway Ave E, Saint Paul, MN, United States
Category
Medical devices › Class II
Classification
Class II
Status
Ongoing
Units affected
186,880 units
Initiated by
Voluntary: Firm initiated

Read the official FDA notice ↗

Product

3M Ranger Irrigation Fluid Warming Set, REF 24750

Why was it recalled?

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

What should you do?

FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.

Product codes & lot numbers

UDI/DI 50707387792720 (box), 10707387792722 (pouch, )SKU 7100235070, All lots with a manufacturing date after March 2022

Distribution

US (nationwide) and Argentina, Australia, Austria, Belgium, Bosnia and Herzegovina, Canada, Canary Islands, China, Costa Rica, Croatia, Czech Republic, 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, Puerto Rico, Qatar, Reunion, Romania, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, Spain, Sweden, Switzerland, Taiwan, Thailand, United Arab Emirates, United Kingdom, Vietnam.

States: Puerto Rico

What does Class II mean?

Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.

Source: FDA (medical devices), recall Z-2231-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.