DOTmed.com
New and Used Medical Equipment For Sale and Wanted
We don't own it... We help you sell it.
My DOTmed
Login | Register
The Medical Industry
Business Weekly
May 08, 2008

Other Headlines

DOTmed was first to break the news late last week that GE's OEC division was given the green light to re-start production; GE says more than 300 OEC® 9900 Elite C-arms are slated to ship within the first 10 days as they start to fill back-orders.
Quinn succeeds Jim Reid-Anderson, who has been named new CEO of Siemens Healthcare.
Account rep Grant Norris is DOTmed Certified.
Normally, three's a crowd. But the trifecta of OEMs, refurbishers and broker/dealers is the engine that's driving the medical trailer business.
Online marketplace for new and used medical equipment reaches another milestone.

Have News for Us?

Submit your news on the industry, people, or companies.

Forward to a Friend

More Industry Headlines

OEC Re-Certified by FDA -- Latest Update DOTmed was first to break the news late last week that GE's OEC division was given the green light to re-start production; GE says more than 300 OEC® 9900 Elite C-arms are slated to ship within the first 10 days as they start to fill back-orders.

SNM Annual Meeting Just About a Month Away The Society of Nuclear Medicine -- SNM -- holds its Annual Meeting this June 14-18 in New Orleans, LA. Exhibitors: You can still get a booth if you hurry!

Medicare Expands Coverage for Artificial Heart Devices Decision opens access to advanced technology.

GE Healthcare Introduces New 3.0T MR Scanner Breakthrough technology with simple design provides radiologists with powerful applications for increased clinical capability.

Get Your Bid in Now on This GE Signa MR/i Hispeed Plus MRI Scanner -- Just Posted on DOTmed! Also see the other great lasers, imaging systems, and more... all on your favorite website for used medical equipment!

Manufacturer of Heart Defibrillator Signs Consent Decree of Permanent Injunction Device manufacturer Physio-Control, Inc., its parent company Medtronic, Inc., and their two top executives have signed a consent decree of permanent injunction related to Automatic External Defibrillators.

Legislative Work Continues on Revamping FDA Congress, Agency say more funding is needed to improve safety.

Healthcare Experts to Address Medical Technology Executives at Annual Conference Medical device industry leaders and key healthcare subject matter experts will meet in Washington, DC for the 2008 Annual Meeting of the Medical Device Manufacturers Association (MDMA).

Wolters Kluwer Health & Johns Hopkins Launch The Patient First journal dedicated to using scientific methods for patient-centric research.

Speaker to Explore Amazing Future of Biotechnology at AAMI Conference Joint Commission executive to provide up-to-date guidance at Association for the Advancement of Medical Instrumentation meeting May 31-June 2 in San Jose, CA.

The Centers for
Disease Control
and Prevention
(CDC)

Cosmetic Soft-Tissue Filler Injections Linked to Cases of Acute Renal Failure

by Astrid Fiano, Writer
The Centers for Disease Control just released a Morbidity and Mortality Report detailing three cases of renal failure linked to soft-tissue filler injections. The cases all occurred in December 2007 in the same Greensboro, North Carolina facility. All three cases of soft-tissue filler injections were performed by persons without medical training or medical supervision.

Soft Tissue Filler Injections are for the purpose of cosmetically-enhancing areas of the face and body. The substances injected in the three cases has not positively been identified. While the facility indicated that the injection ingredient was liquid silicone, liquid silicone has not been associated in the past with acute renal failure.

One 42-year-old female patient received two sets of injections in her buttocks within a two-week period; a couple of days after the second injection the patient reported to an emergency department with fatigue, vomiting, and headache and was found to have acute renal failure. A second 26-year-old female patient received at least two sets of injections in the buttocks. Shortly after the last set she went to an emergency department with nausea, headache, and fatigue and was also found to be in acute renal failure. The third patient, another 26-year-old, received two sets of injections in the buttocks, and a few days after the second set reported to an emergency department with fatigue and vomiting. She was found to have acute interstitial nephritis. All three patients were known to be previously healthy.

The Guilford County Health Department investigated the facility and found several violations of infection-control practices. In addition, the Department discovered the patients were not given information on the risks of soft-tissue filler injections. While the practitioner in the facility claimed the substance injected was silicone oil, no evidence to support the claim was given to the Department.

Following local press reports, more complaints were lodged with the Department concerning the facility. Five persons called the Department to complain of injection-site reactions including inflammation, abscesses and pulmonary embolism. The facility practitioner was later arrested and charged with practicing medicine without a license.

Since the cluster of soft-tissue filler injections was posted on the CDC's Epidemic Information Exchange in December of 2007, no other cases have yet been reported. The CDC report emphasizes the risk to consumers receiving cosmetic injections from facilities without medically trained or supervised personnel.

More information available at: http://www.cdc.gov/mmwR/preview/mmwrhtml/mm5717a1.htm

Please Send us your Comments.

Access and use of this site is subject to the terms and conditions of our LEGAL NOTICE & PRIVACY NOTICE
Property of and Proprietary to DOTmed.com, Inc.
Copyright ©2001-2008 DOTmed.com, Inc.
ALL RIGHTS RESERVED