Zimmer Biomet Hip Replacement Recall

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‍Zimmer Biomet CPT Hip System Recall: Are You Suffering Due to a Defective Implant?

Pittman, Dutton, Hellums, Bradley & Mann, P.C. is currently representing individuals who have experienced complications or required revision surgery due to the defective Zimmer Biomet CPT Hip System. Recent research has highlighted the increased risk of post-surgical thigh fractures associated with this hip implant, leaving many patients in need of additional corrective procedures.

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Zimmer Biomet Issues a Recall for CPT Hip System

On July 2, 2024, Zimmer Biomet announced a voluntary recall of its CPT Hip System Femoral Stem with a 12/14 Neck Taper. Despite acknowledging the defect, the manufacturer plans to continue selling the remaining units until the end of the year. This decision puts countless patients at risk of experiencing avoidable complications.

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Increased Risk of Thigh Fractures

Clinical research has shown that the Zimmer Biomet CPT Hip System poses a significantly higher risk of postoperative thigh fractures compared to similar hip implants. The fracture risk with this system is 1.4%, while other devices range between 0.6% and 1.0%. Thigh fractures often cause severe pain and typically require revision surgery, which is more complex and riskier than the initial procedure.

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What the Recall Means for You

If you received the Zimmer Biomet CPT Hip System, you may experience complications such as:

• Thigh pain
• Difficulty walking or limited mobility
• Fractures in the femur

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These issues often necessitate revision surgery, which carries additional risks, including:

• Infection
• Blood clots
• Nerve damage
• Implant loosening
• Unequal leg length
• Pulmonary embolism
• Dislocation of the implant
• Heart attack or stroke

Revision surgery is not only more complicated than the initial hip replacement but can also significantly impact your overall health and quality of life.

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Holding Zimmer Biomet Accountable

Manufacturers of medical devices have a duty to ensure their products are safe for patients. Zimmer Biomet’s decision to issue a recall while still selling defective implants is deeply concerning and highlights the need for accountability. Patients should not have to endure unnecessary pain, suffering, and surgical risks due to corporate negligence.

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Our Experience in Medical Device Litigation

At Pittman, Dutton, Hellums, Bradley & Mann, P.C., we have a proven track record of holding medical device manufacturers accountable. Our legal team has successfully represented clients in cases involving defective hip implants, helping them secure compensation for their injuries, medical expenses, and pain and suffering.

We understand the physical, emotional, and financial toll that a defective medical device can have on your life. Our goal is to fight for justice and ensure you receive the compensation you deserve.

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What You Should Do Next

If you have experienced complications or required revision surgery due to a Zimmer Biomet CPT Hip System, you are not alone. Our experienced attorneys are here to help you understand your legal options and guide you through the process.

Contact us today for a free consultation at (205) 322-8880. We are committed to helping you hold Zimmer Biomet accountable and achieve the justice you deserve.

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LINKS:

[1] https://www.fda.gov/medical-devices/safety-communications/zimmer-biomet-cpt-hip-system-femoral-stem-and-increased-risk-thigh-bone-fracture-fda-safety