3M recalls blood/fluid warming sets with catalog numbers 24355 and 24370 made after March 2022 due to unclear flow rate and temperature specifications.
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.
3M is recalling blood and fluid warming sets with catalog numbers 24355 and 24370 that were made after March 2022. The issue is that the flow rates and temperature readings may not be clear, which could lead to improper use during medical procedures.
The sets may have unclear flow rate and temperature specifications, which could lead to improper use during medical procedures. This might affect the effectiveness of the warming process but does not pose an immediate safety risk.
Healthcare professionals using these warming sets for blood or fluid treatments are likely affected. Those with the specific catalog numbers and manufacturing dates after March 2022 are most at risk.
Check the catalog number on the product, which should be either 24355 or 24370. The product was manufactured after March 2022.
Verify the catalog number and manufacturing date to confirm if the product is affected.
The recall is due to unclear flow rate and temperature specifications for the blood/fluid warming sets, which could affect proper use during medical procedures.
Check the catalog number and manufacturing date. If it matches the affected items (catalog numbers 24355 or 24370 made after March 2022), you should verify the specifications with 3M.
The recall does not include a fix; it requires users to check the product details and ensure proper use based on the updated specifications.
We’ve drafted a message you can send 3M to request your refund or repair — edit it as you like.
Subject: Recall Z-2483-2025 — 3M 3M Hello, I own a 3M that is covered by recall Z-2483-2025 from 3M. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
