FDAJanuary 24, 2018device

Liberty Select Cycler (SW v.2.8.7), Material Number RTLR108343 Product Usage: The device is indicated for acute and chronic peritoneal dialysis.

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

The hazard

The recalling firm identified a software issue related to the Patient Line Check (PLC) which may result in an increased risk of Overfill (also known as Increased Intraperitoneal Volume, IIPV). Overfill/IIPV may result in serious injury or death.

What to do

FDA enforcement status: Terminated

Brands named

fresenius medical care renal therapiesfreseniusfresenius medical

Recall history

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

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