19 Jan

The Stryker Corporation announced a recall of two of its hip implant systems in July of 2012. The company is facing a growing number of lawsuits filed by patients with the recalled device, some of whom have suffered painful tissue death, bone […]

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19 Jan

The FDA recently designated three medical devices made by CareFusion, Johnson & Johnson, and Teleflex as Class 1, meaning that there exists a reasonable probability that the use of or exposure to the devices will cause serious adverse health effects or possibly […]

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