2016 ESRD Facility Surveys (CMS-2744 Form) are due to Midwest Kidney Network on March 31, 2017.  Please have them submitted for ESRD Network review and acceptance by that date.

January 11, 2017

The FDA has identified a Class II recall for the Tego Connector, Item No. D100, NM1000 The Tego Needle Free Access Device.

January 5, 2017

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.

Recalled Product: