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Individuals Who Had A Total Hip Replacement After 2018 Using Synovo Total Hip Replacement Systems And Devices May Be Eligible For Justice And Potential Compensa

Seeger Weiss is investigating claims of device failure in Synovo Total Hip Replacement System devices:

  • Endotec BP devices
  • Synovo Preserve
  • Synovo Total Hip Replacement System

The Potential For Synovo Hip Implant Complications After A Total Hip Replacement Surgery

You may be eligible for compensation if you had a total hip replacement after 2018 using:

  • Endotec BP devices
  • Synovo Preserve
  • Synovo Total Hip Replacement System

The FDA has issued a “Do Not Use” warning regarding Synovo Total Hip System devices, including:

  • Acetabular Bearing
  • Acetabular Fixation Cup
  • Femoral Resurfacing Cup

Seeger Weiss is investigating claims of device failure in Synovo Total Hip Replacement System devices.

iStock-1458728507

FDA Synovo Hip Warning

The U.S. Food and Drug Administration (FDA) warned Surgeons and Surgical Centers regarding Synovo Total Hip Replacement System Devices. Synovo Total Hip Replacement System has also been known as Synovo Preserve and Endotec BP.

The January 2024 warning advises that Synovo Total Hip System devices manufactured after 2018 should not be used in hip implant procedures and states that the devices may not meet FDA guidelines.

The FDA recommends that devices should not be purchased or implanted and that they be removed from inventory due to a high risk of device failure.

Complications Linked to Synovo Hip Replacement Devices

A higher-than-expected risk of complications and adverse events has been linked to the use of the Synovo Total Hip Replacement System components.

Patients have reported symptoms including:

  • Grinding or other noises
  • Hip weakness
  • Inability to bear weight
  • Increasing pain
  • Knee weakness
  • Loosening hardware

The FDA has not recommended that the devices be removed from patients who are not experiencing difficulties but has recommended that patients should be closely monitored and that symptoms be reported to a health provider immediately.

People who received a Synovo Total Hip Replacement System and experienced complications or required hip revision surgery may be eligible for compensation.

Eligible victims are encouraged to request a free, private case evaluation by our experienced legal staff with the potential for compensation and justice.

Find Out if You Qualify

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The Potential For Synovo Hip Implant Complications After A Total Hip Replacement Surgery

You may be eligible for compensation if you had a total hip replacement after 2018 using:

  • Endotec BP devices
  • Synovo Preserve
  • Synovo Total Hip Replacement System

The FDA has issued a “Do Not Use” warning regarding Synovo Total Hip System devices, including:

  • Acetabular Bearing
  • Acetabular Fixation Cup
  • Femoral Resurfacing Cup

Seeger Weiss is investigating claims of device failure in Synovo Total Hip Replacement System devices.

iStock-1458728507

FDA Synovo Hip Warning

The U.S. Food and Drug Administration (FDA) warned Surgeons and Surgical Centers regarding Synovo Total Hip Replacement System Devices. Synovo Total Hip Replacement System has also been known as Synovo Preserve and Endotec BP.

The January 2024 warning advises that Synovo Total Hip System devices manufactured after 2018 should not be used in hip implant procedures and states that the devices may not meet FDA guidelines.

The FDA recommends that devices should not be purchased or implanted and that they be removed from inventory due to a high risk of device failure.

Complications Linked to Synovo Hip Replacement Devices

A higher-than-expected risk of complications and adverse events has been linked to the use of the Synovo Total Hip Replacement System components.

Patients have reported symptoms including:

  • Grinding or other noises
  • Hip weakness
  • Inability to bear weight
  • Increasing pain
  • Knee weakness
  • Loosening hardware

The FDA has not recommended that the devices be removed from patients who are not experiencing difficulties but has recommended that patients should be closely monitored and that symptoms be reported to a health provider immediately.

People who received a Synovo Total Hip Replacement System and experienced complications or required hip revision surgery may be eligible for compensation.

Eligible victims are encouraged to request a free, private case evaluation by our experienced legal staff with the potential for compensation and justice.

100% Free & Secure Case Evaluations

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We’ll ask specific questions to understand the situation, the injuries, and other vital info to help determine the next steps.

Receive a confidential case evaluation

A qualified legal team led by a personal injury attorney will consider the facts of the case and the potential for compensation.

File An Individual Claim for Compensation

Those who qualify will have an individual claim filed in a court of law for the justice and compensation they deserve.

You no longer have to suffer from the personal injury linked to the use of the Synovo Total Hip Replacement System—we will stand with you and fight for justice!

We encourage people who received a Synovo Total Hip Replacement System and experienced complications or required hip revision surgery to request a free, private case review to qualify for potential compensation.

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