FDAAugust 27, 2019device

Low Volume Cartridge IFU (SKU CAR-125-B) used with the following devices: 1) NxStage One, Model NX1000-1; 2) NxStage VersiHD Cycler, Model Numbers: NX1000-16, and NX1000-16-A; 3) NxStage One, Model Numbers: NX1000-3 and NX1000-3-A; 4) NxStage One, Model Numbers: NX1000-10 and NX1000-10-A;

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

The hazard

There is a potential patient health risk while performing chronic hemodialysis treatments in the home setting with for patients with low blood volume (2.4 Liters or less in a patient with body weight of 30kg or less) when prescribing larger dialysate volumes.

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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