FDADecember 15, 2015device

Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and RTLR180111

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

The hazard

The door latch may not fully close and the door may open unexpectedly. The door may make physical contact with anything near the door of the machine, including the patient. May cause injury, delay in treatment, or Increased Intraperitoneal Volume (IIPV) (overfill).

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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