Recall: Fresenius Liberty Cyclers

The FDA has announced a Class II recall of all Fresenius Liberty Peritoneal Dialysis Cyclers, models 180111 and RTLR180111 because of malfunctioning doors that may disrupt treatment.  For details see http://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-0693-2016&w=02032016&lang=eng .

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