February 2, 2017
January 25, 2017
January 24, 2017
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.
The Centers for Medicare & Medicaid Services (CMS) would like to notify facilities that PY 2017 Performance Score Certificates (PSC) will be available for download on December 15, 2016.
November 8, 2016