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

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.

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

Individuals who had a total hip replacement after 2018 using Synovo Total Hip Replacement Systems and devices may be eligible for justice and potential compensation.

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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!

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

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

Our attorneys are experienced in medical and healthcare litigation and know how to encourage stubborn companies to make a real offer of compensation to cover the personal injury linked to the use of the Synovo Total Hip Replacement System, which resulted from the manufacturer's negligence.

Details On The Complications Linked to Synovo Hip Replacement Devices

What are the details of the U.S. Food and Drug Administration (FDA) Synovo hip warning?

The FDA warned surgeons and surgical centers of the dangers of Synovo Total Hip Replacement System Devices, which have also been known as Synovo Preserve and Endotec BP.

Patients have reported symptoms including:

Grinding or other noises

Hip weakness

Inability to bear weight

Increasing pain

Knee weakness

Loosening hardware

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

Acetabular Bearing

Acetabular Fixation Cup

Femoral Resurfacing Cup

Endotec BP devices

Synovo Preserve

Synovo Total Hip Replacement System

Compensation Begins With A Free Online Case Review

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.

Synovo Total Hip Replacement System FAQ: Questions About The Synovo Total Hip System & Elements

What are the details of the most recent warning from the FDA?

The January 2024 warning advises that Synovo Total Hip System devices manufactured after 2018 should not be used in hip implant procedures.

What are the recommendations for those considering using or purchasing these devices?

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

What are the FDA recommendations for patients who are not experiencing difficulties?

The FDA has recommended that patients be closely monitored and symptoms be reported to a health provider immediately.

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