FDAJanuary 29, 2024device

NxStage Cartridge Express with Speedswap, Catalog No. CAR-535. An accessory device for facilitating the removal and replacement of a flow-compromised filter during treatment of acute and chronic renal failure or fluid overload.

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

The hazard

Product is recalled due to reports of blood leaking or spraying from the arterial line on the cartridge.If this failure occurs, a patient may experience uncontrolled blood loss or a healthcare professional could be exposed to infectious patient blood.

What to do

FDA enforcement status: Ongoing

Brands named

nxstage mdsnxstage

Recall history

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

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