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Synovo Lawsuits Surge over Total Hip System after the FDA Safety Alert

In recent years, individuals who underwent hip replacement surgery using Synovo's modified components have found themselves facing unexpected challenges. The FDA has identified three modified components, which must have been manufactured after 2019, raising concerns about the safety of Synovo's hip replacement systems.

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Synovo Lawsuits Surge over Total Hip System after the FDA Safety Alert

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  1. Elementary School Presents Synovo Lawsuits: Total Hip System Implants Face FDA Warning

  2. FDA warning on January 3, 2024 shocked medical community and patients • Focus light fell on Synovo Hip System

  3. In March 2023 FDA warned Synovo for unauthorized modifications to Synovo Hip System • Components affected: Femoral Resurfacing Cup, Acetabular Fixation Cup, Acetabular Bearing

  4. Modifications shifted devices to cementless fixation • Changes were not submitted for the FDA approval • Potential risks: potential loosening, revision surgeries

  5. FDA's warned Synovo of: • Misbranding, adulteration, quality system regulation violations • Patient safety at risk

  6. FDA advised healthcare providers to stop using modified implants • Monitor patients for device failure • Surge in lawsuits from affected patients loom • Synovo lawsuits seek justice and compensation

  7. Want to substantiate claims? • Consult with experienced attorneys • Ensure medical records are thoroughly reviewed

  8. For a flawless medical record Contact Phone: +1-404-382-5426 Mail: sales@lezdotechmed.com Web: https://www.lezdotechmed.com/

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