News and Updates

Category: Defective Devices

NeuroBlate System

NeuroBlate Timeline of Key Events

  April 1, 2013 – FDA cleared the NeuroBlate System for use in the U.S. It’s important to note that the NeuroBlate System was never approved by the FDA. Instead, it was merely “cleared” by the 510(k) process, meaning the FDA permitted Monteris to market the device because it was substantially equivalent to a device…

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Pelvic Mesh

Pelvic Mesh Manufacturer Settles For $750 Million

For women suffering from pelvic mesh complications, holding the manufacturers responsible for their defective devices is incredibly important. Luckily, for some victims, a resolution to their claims has finally arrived. One popular pelvic mesh manufacturer, Endo International PLC, has agreed to pay $750 million to settle 22,000 pelvic mesh lawsuits.

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