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Qui tam lawsuits are a form of civil lawsuit whistleblowers file under the False Claims Act. This act is a federal law that rewards whistleblowers if their qui tam case(s) recover funds for the government.

The US Food and Drug Administration (FDA) has announced the Class I recall of HeartMate II implantable heart pumps over a controller issue, after the devices have been linked to four patient deaths and five

The Baxter Vascular Patch for peripheral vascular reconstruction is involved in a product recall. A FDA Class I recall is “a situation in which there is a reasonable probability that the use of or exposure

According to the Chicago Tribune, Baxter Healthcare Corp is recalling multiple models of infusion pumps used to deliver medicine, blood and other fluids after it received over 3,500 reports of the product malfunctioning.The U.S. Food and Drug

Recently, Johnson & Johnson recalled multiple lots of jaw implants after they were reportedly linked to more than a dozen injury cases. According to Fox News, the device, known as the Craniomaxillofacial Distraction System, is used to