3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355 — Class I medical device recall Z-2483-2025
Ongoing recall by 3M Company, reported 2025-09-24, distributed nationwide. Field action to clarify the flow rates and inlet fluid temperatures, along with location of the outlet tempera
| Recall number | Z-2483-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | 3M Company, Saint Paul, MN, United States |
| Recall initiated | 2025-04-10 |
| Classified | 2025-09-18 |
| Reported by FDA | 2025-09-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BE, CA, CH, CN, CR, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HK, HR, HU, IE, IL, IT, JO, KR, LU, NL, NO, NZ, PL, PT, QA, RO, RS, SA, SE, SG, SI, SK, TH, TW, VN |
| Quantity | 530,470 units |
| Model numbers | 24355, 24370 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2483-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.