News

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:

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.

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