Cases we work on
Medical devices, products, and equipment are created to improve the health and wellbeing of patients, however, poor design, quality, and manufacturing can result in dangerous and deadly defects.
Our LNCs screen cases, allowing them to quickly identify whether or not a case is qualified by identification of the device product ID (lot number, sticker sheet, etc.), verification of proper placement (per manufacturers guidelines), and any complications/issues reported on the day of placement.
LNCs review and analyze all medical records for evidence of post-device placement complications and evidence of device malfunction/migration including lab work, diagnostic tests, office visits, medications, treatments, revisions, removals, etc.
Our staff will assess all aspects of an individual’s medical history that may have possibly contributed to the alleged post-device placement symptoms they are experiencing. We can assist with creating complete timelines of the medical history, preparing the attorney for any prior medical history or issues that may be brought up during deposition.
Defective drugs and manufacturer errors can lead to serious health conditions and even death.