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Recall Observatory FDA recall evidence

Device product

PRISMAFLEX HF1000 SET, Product Code 107142; Dialyzer, High Permeability With Or Without Sealed Dialysate System

Z-1230-2026

January 06, 2026

Class II

Product summary

Firm
VANTIVE US HEALTHCARE LLC
Event
Event 98180
Status
Ongoing
Classification
Class II
Quantity
115,112 units
Official record key
device-enforcement:Z-1230-2026

Official wording

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

Code information: UDI/DI 07332414069315, All lots including and manufactured after 24F0094CA

Distribution pattern: US Nationwide distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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