Reasons the FDA Has Sited for Hip Replacement Recalls
Ohio Personal Injury Attorney, Thomas P. Maney handles Knee Replacement Defective Product Injury cases for victims throughout the State of Ohio. Contact our office for a confidential legal consultation.
Call Toll Free: 800.848-LAWS (5297) to discuss your Knee Replacement Defective Product Injury Case.
When the FDA urges or forces a company to issue a recall, the FDA identifies the specific issue with the hip replacement device and components, and the injuries that are known to have been documented as a result of the defect. Known side effects identified by the FDA for hip replacement recalls include:
- Joint infection
- Bone fracture
- Hip dislocation
- Osteolysis, or bone loss
- Loosening or breaking of the device
- Nerve damage resulting in weakness or numbness
- Differences in the length of a patient’s legs
As you can see, not all of the conditions or reasons that you can file a lawsuit against the hip replacement designer, manufacturer or parent company is listed as a reason for recall. The recall standards are just a general list of noted reasons for a recall for these devises, and by no means limits your ability to file a defective product or personal injury civil litigation case.
Call Toll Free: 800.848-LAWS (5297) to find out how we may be able to help you with your Knee Replacement Defective Product Injury Case.
We handle Knee Replacement Defective Product Injury cases for victims in Columbus, OH, Cincinnati, Dayton, Toledo, Cleveland, Youngtown, Akron, Canton, and throughout the State of Ohio.
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