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Latest Synovo Hip Lawsuit Updates

People who received Synovo Total Hip System implants are filing lawsuits against the company following a U.S. Food and Drug Administration Safety Warning. The FDA found significant alterations in devices produced since 2019 that deviated from the FDA-approved design.

Latest Synovo Hip Lawsuits Developments
  • January 2024:
    The FDA advises health care providers to avoid using the Synovo Total Hip Resurfacing System due to significant modifications made to the device, which differ from the version initially approved by the FDA.
  • March 2023:
    The FDA sends a Warning Letter to Synovo stating that the company has violated numerous regulations. The letter instructs Synovo to stop the production of modified devices immediately and promptly address all the violations mentioned in the letter.
  • 2019
    Synovo changes its Total Hip Replacement System without obtaining clearance from the FDA.

While litigation is still in its early phases, there are no noteworthy settlements or jury decisions yet. Nevertheless, personal injury attorneys are actively accepting cases related to Synovo hip complications.

FDA Safety Warning About Synovo Total Hip Resurfacing System

In 2024, the FDA issued a safety communication about Synovo’s Total Hip Resurfacing System. The agency criticized substantial modifications made to the components since 2019.

If you received an implant after 2019, the FDA recommends you monitor it regularly with your health care provider. The FDA discourages removal and replacement surgery unless necessary.

“Contact your health care provider if you experience any symptoms such as new or worsening pain, loosening, grinding or other noise, inability to bear weight, or weakness of the hip or knee on the side of your implant.”
FDA Safety Communication, Jan. 3, 2024

The FDA warned health care providers against using the Synovo Total Hip System and advised doctors and patients to report any problems through the MedWatch Voluntary Reporting Form. The FDA has also requested that Synovo inform its customers about the risks associated with their devices and meet FDA requirements.

Other Recent Hip Replacement Lawsuits

As of February 2024, 1,169 Exactech lawsuits were pending in multidistrict litigation before the Eastern District of New York. No trials or approved settlements have been reported regarding MDL 3044. The number of cases is steadily increasing as lawyers accept new ones.

Since 2010, tens of thousands of hip replacement lawsuits have been filed against at least seven major manufacturers, resulting in multidistrict litigations and billions of dollars in jury verdicts and settlements.

Why Do People File Synovo Total Hip Lawsuits?

People are filing Synovo hip lawsuits because of FDA concerns regarding modifications made to several Synovo Total Hip System components.

“The safety and effectiveness of the Synovo Total Hip System, including the Femoral Resurfacing Cup, the Acetabular Fixation Cup, and the Acetabular Bearing, have not been established.”

Modifications to Snyovo hip implants can cause pain and device malfunction, leading to costly revision surgeries exceeding $40,000. Lawsuits can help patients receive compensation for injuries and revision surgery.

Health Concerns Over Synovo Total Hip Systems

The most serious health concern over the Synovo Total Hip System is failure, which can require revision surgery. This involves removing and replacing a faulty hip implant. These surgeries may take more time in the operating room and under anesthesia than the original hip replacement procedure.

Reasons for Revision Surgery
  • Allergy to materials in the implant
  • Bone fractures
  • Device failure
  • Dislocation
  • Implant wear
  • Infection

In addition, there are other signs and complications you should be aware of if you have received a Synovo hip implant since 2019.

Signs of Synovo Total Hip Resurfacing System Issue
  • Weakness of the hip or knee on the side of your implant
  • Pain
  • Loosening
  • Inability to bear weight
  • Grinding or other noise

The FDA recommends that you contact your health care provider if you experience any of these problems.

Who Qualifies for a Synovo Lawsuit?

You may be eligible to file a lawsuit if you received a Synovo hip replacement and required revision surgery or experienced pain or other side effects.

You must have received a Synovo Total Hip Replacement System or other company brand using any of the three modified components identified by the FDA. The components must have been manufactured after the modifications took place in 2019.

Affected Synovo Hip Brands
  • Endotec BP
  • Synovo Preserve
  • Synovo Total Hip Replacement System

If you pursue a Synovo lawsuit, you may have specific eligibility requirements. However, since only a lawyer can confirm your eligibility, it is crucial to schedule a free consultation with a Synovo lawsuit attorney as soon as possible.

Depending on the lawyer you choose, you may need to meet certain eligibility criteria to file a Synovo hip replacement lawsuit.

How To File a Synovo Hip Lawsuit

If you are planning to file a Synovo hip lawsuit, consider hiring a skilled attorney willing to take on big medical device companies. With most mass torts law firms, you can schedule a free consultation to learn about your options to protect your rights and get the compensation you deserve.

During the interview, ask about the firm’s success in obtaining settlements or jury verdicts for clients injured due to recalled defective medical devices. A lawyer from a national law firm with adequate resources and experience may be the most suitable option in case Synovo hip lawsuits are consolidated into multidistrict litigation.

Please seek the advice of a qualified professional before making decisions about your health or finances.
Last Modified: February 7, 2024

8 Cited Research Articles

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  1. Brockenbrough, G. (2024, January 4). FDA Advises Against Use of THA System Due to Significant Modification. Retrieved from https://www.healio.com/news/orthopedics/20240104/fda-advises-against-use-of-tha-system-due-to-significant-modification
  2. Hobbins, K. (2023, January 4). FDA Warns Against Using Synovo Total Hip System. Retrieved from https://www.mddionline.com/regulatory-quality/fda-warns-against-using-synovo-total-hip-system
  3. Hale, C. (2024, January 4). FDA Warns Against Using Synovo Total Hip Replacement Implants. Retrieved from https://www.fiercebiotech.com/medtech/fda-warns-against-using-synovo-total-hip-replacement-implants
  4. Whooley, S. (2024, January 3). FDA Says Not To Use Certain Hip Implants From Synovo. Retrieved from https://www.massdevice.com/fda-dont-use-hip-implants-synovo/
  5. U.S. Food and Drug Administration. (2024, January 3). Do Not Use Synovo Total Hip Resurfacing System: FDA Safety Communication. Retrieved from https://www.fda.gov/medical-devices/safety-communications/do-not-use-synovo-total-hip-resurfacing-system-fda-safety-communication
  6. U.S. Judicial Panel on Multidistrict Litigation. (2024, January 2). MDL Statistics Report. Retrieved from https://www.jpml.uscourts.gov/sites/jpml/files/Pending_MDL_Dockets_By_Actions_Pending-January-2-2024.pdf
  7. Schulte, F. (2023, October 10). Thousands Got Exactech Knee or Hip Replacements. They, Patients Say, the Parts Began to Fail. Retrieved from https://www.cbsnews.com/news/exactech-knee-hip-replacements-lawsuits/
  8. U.S. Food and Drug Administration. (2023, March 23). Warning Letter; Synovo Production, Inc. Retrieved from https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/synovo-production-inc-647427-03232023