ClearanceBrief
Recall Z-2439-2025 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

VANTIVE US HEALTHCARE LLC

TherMax Blood Warmer Unit-US, PrisMax Accessory, Product Codes: 955630, 955515, 955702, 955631

DateAug 26, 2025 (initiated Jul 28, 2025)
StatusOpen, Classified
ReasonThermax System may be unable to detect the presence of a bag on the Thermax Blood Warmer Unit leading to difficulty setting up therapy, or PrisMax System alarm T2284: Thermax Disposable Not Inserted
Root causeUnder Investigation by firm
ActionVantive issued an Urgent Medical Device Correction notice to it consignees on 0728/2025 via USPS first class mail. The notice explained the issues with the devices, hazard involved, and requested the following: Actions to be Taken by Customers 1. Operators may continue to safely use the PrisMax Systems and TherMax Blood Warmer Units per the associated Operator s Manuals and on-screen instructions. If further assistance is required, please contact your local Vantive account representative. Please ensure that all operators of these devices are made aware of this Urgent Medical Device Correc
Quantity7432 units
DistributionWorldwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K190910PrisMax System Version 2
Baxter Healthcare Corp, Jul 25, 2019
K193482PrisMax System Version 3
Baxter Healthcare Corporation, Mar 13, 2020