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Recall Observatory FDA recall evidence

Device product

PRISMAFLEX M150 SET, Product Code 109990; Dialyzer, High Permeability With Or Without Sealed Dialysate System

Z-1228-2026

January 06, 2026

Class II

Product summary

Firm
VANTIVE US HEALTHCARE LLC
Event
Event 98180
Status
Ongoing
Classification
Class II
Quantity
137,576 units
Official record key
device-enforcement:Z-1228-2026

Official wording

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

Code information: UDI/DI 07332414090005, All lots including and manufactured after 24F0100CA

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.