Auxo Medical News

The ban is effective January 18, 2017

Here’s a reminder of the recent ban of powdered gloves by the Federal Drug Administration (FDA). Compliance is mandatory in less than a week.

Bottom-Line

In its announcement last month, the FDA formally banned two types of powdered gloves and a glove lubricant. These medical devices can no longer be legally marketed or used effective January 18, 2017. That prohibition applies to devices already in commercial distribution and those sold to the end user.

Specifically, the ban applies to powdered patient examination gloves, powdered surgeon’s gloves and absorbable powder used to lubricate surgeon’s gloves. The glove types include all of these gloves, regardless of the material from which they are made – including NRL and synthetic latex gloves.

Hospitals data base systems are being hacked.

It’s been all over the news … hospitals being hacked, data held hostage and ransom paid to the perps. Hollywood Presbyterian Medical Center and MedStar Health in D.C. are two recent victims that have been prominently in the press and paid significant dollars to cyber bandits.

And Compelling Reasons Why 

Total Knee Arthroplasty may be removed from the Medicare Inpatient Only list.

In 2000 the Centers for Medicare & Medicaid Services (CMS) added Total Knee Arthroplasty (TKA) to the Medicare Inpatient Only (IPO) list in 2000. More than a decade later, in 2013, the CMS proposed that the procedure be removed from the IPO list in anticipation that some Medicare beneficiaries would be well served in an outpatient environment. There was considerable adverse public reaction to this proposed move so it was not finalized at that time.

Now, three years later, the CMS is once again considering removal of TKA from the IPO list and soliciting public comments on that proposal. Driving this effort are two prime factors:

HELP Is On The Case

Looking at the current state of proposed healthcare Information Technology (IT) reforms as unanimously passed by the HELP Committee.

Healthcare increasingly is a patient-centered world where information technology (IT) has a major effect on diagnosis and personalized treatments. Without a doubt, electronic health record (EHR) technology is under significant scrutiny by the U.S. Senate Committee on Health, Education, Labor and Pensions (HELP).

For over a year, the HELP committee has been investigating potential issues with health IT and the meaningful use of certified EHR systems. An important development occurred in February of this year when HELP voted unanimously to pass the Improving Health Information Technology Act (S. 2511).

View the the current version as revised in April of this year.