Starting with the basics, the recall was issued by AvKARE - HealthKARE Solutions for Tomorrow, a company that distributes a variety of pharmaceuticals, medical & surgical items ... in their inventory ...

Studies evaluating surgical-site infection have had conflicting ... reoperation for fracture-healing complications. Download a PDF of the Research Summary. A total of 6785 patients with a closed ...

The recall was for over 21,000 electro-surgical tools due to serious risks. The tools were from Johnson & Johnson's Mega 2,000 and Mega soft reusable electrodes, which are electric pads used to ...

The agency classified the recall on Tuesday as 'most serious.' The tools, which were sold under the brand names MEGA 2000 and MEGA SOFT Reusable Patient Electrodes, were recalled by Utah-based ...

In the NHTSA's letter (PDF) to ARC urging the company to issue a recall, it listed nine incidents wherein a driver (and, in some cases, a passenger) had been injured because an inflator had ruptured.

A rare strain of bacteria found in recalled eyedrops has been linked to dozens of infections, as well as cases of vision loss, surgical removal ... initiated a voluntary recall last month, and ...