FDA Enforcement Class II Ongoing

PRISMAFLEX ST150 SET US, Product Code 107640US; Dialyzer, High Permeability With Or Without Sealed Dialysate System

Recall: Z-1225-2026 · Reported February 11, 2026

Enforcement

Recall Number
Z-1225-2026
Event ID
98180
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
VANTIVE US HEALTHCARE LLC
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
February 11, 2026
Initiation Date
January 6, 2026
Classification Date
February 2, 2026
Address
510 Lake Cook Rd, N/A, Deerfield, IL, 60015-4964, United States

Description

PRISMAFLEX ST150 SET US, Product Code 107640US; Dialyzer, High Permeability With Or Without Sealed Dialysate System

Reason

There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.

Code Info

UDI/DI 00085412917696, All lots including and manufactured after 24F0085

Distribution

US Nationwide distribution.

Quantity

264,040 units