FDAOctober 29, 2015device

NxStage System One S Cycler -High Permeability Hemodialysis System Model no. NX1000-4

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Ultrafiltration Volume (UFV) may not decrease during treatment-software error. The UF pump may continue to run and remove fluid even after the target UF volume has been removed

What to do

FDA enforcement status: Terminated

Brands named

nxstage medicalnxstage

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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