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Loana Edmonds received a spinal pain stimulator implant in 2018, which was recently identified as part of an official medical device recall. She has since experienced worsening pain, functional complications, and overall decline in her condition, prompting her current doctor to recommend full removal of the implant. A corrective surgery is scheduled for April 14, 2025, with no confirmation yet as to whether her medical provider will cover the procedure’s cost. Loana is primarily interested in pursuing a product liability claim against the manufacturer of the recalled implant, citing physical suffering and disruption to her quality of life. While her doctor acknowledged the device must be removed due to its failure, she is still unsure whether the hospital or insurance will take responsibility for her medical expenses. She also confirmed that her device’s serial number matches one on the official recall list, providing a clear foundation for liability. She has preserved key documentation, including the original product packaging and recall details, which will help substantiate her claim. Loana appears cooperative and ready to proceed, and her situation presents a compelling case of manufacturer negligence with the potential for escalating medical costs and long-term damage. If the hospital declines coverage, additional liability concerns may extend to her care provider as well.