Hip replacement surgeries have become a common and sought-after procedure for many people dealing with severe hip pain or mobility issues. For those who’ve lived with the discomfort of hip-related problems, these surgeries are supposed to offer a new lease on life.
Among the various hip replacement systems available, the Zimmer Biomet CPT Hip System has been designed to help many individuals achieve this better quality of life. However, the FDA recently issued a serious safety alert about an increased risk of thigh bone fractures following surgery with this particular hip system.
Keep reading to learn more about the Zimmer Biomet recall and what it means for patients who are considering the device or already have it implanted.
This is the latest in a frustrating string of issues tied to Zimmer hip replacement devices. If you are one of the many who have experienced a thigh bone fracture due to a defective Zimmer Biomet CPT, Meshbesher & Spence can help.
Contact us online or call (612) 339-9121 to understand your legal options and how we can support you in filing a claim. We have decades of experience in helping those dealing with orthopedic device failure.
What Is the Zimmer Biomet CPT Hip System?
The Zimmer Biomet CPT is a hip replacement system that has been used clinically for more than 25 years. One important part of this medical device is the CPT Hip System Femoral Stem. This component is made from a very strong material called cobalt-chromium alloy.
It’s designed to be durable and long-lasting, which is important for a hip replacement and what makes these incidents all the more infuriating. The stem is shaped to fit inside the thigh bone (femur) and helps hold the new hip joint in place.
About the Zimmer Biomet CPT Hip System Failure
On September 17, 2024, the U.S. Food and Drug Administration (FDA) issued a critical safety alert regarding the Zimmer Biomet CPT Hip System. This communication is a serious wake-up call for patients and healthcare providers.
The FDA’s communication reveals a significant and troubling oversight: an increased risk of thigh bone fractures, known as postoperative periprosthetic femoral fractures, associated with the CPT Hip System.
The Problem With Femoral Fracture After Hip Replacement
This risk means that after already undergoing hip replacement surgery with this device, patients are more likely to experience fractures around the thigh bone.
It’s important to note that this recall isn’t just a minor inconvenience for patients. Instead, these fractures can lead to severe pain, further surgeries, and extended recovery times. Therefore, the Zimmer Biomet CPT Hip System and thigh fracture risk is a serious concern that should not be taken lightly.
Is There a Zimmer Biomet Recall?
In July 2024, Zimmer Biomet announced a voluntary recall. However, the main focus of this recall was to update the instructions for the CPT Hip System. The company has announced plans to phase out the sale of the CPT Hip System entirely by December 2024.
While this decision might seem like a responsible move, it does little to address the immediate concerns of the many patients who have already undergone surgery with this problematic device.
Additionally, the FDA raised concerns about the hip implant continuing to be implanted in new patients, even with updated instructions. These worries were heightened by recent research that found this device has a higher risk of thigh bone fractures than similar hip replacement devices.
That’s why the FDA felt it needed to notify the public about the Zimmer Biomet CPT Hip System and thigh fracture risk through the latest safety communication.
Study Reveals Alarming Risks Linked to Zimmer Biomet CPT Hip System
An analysis by the Medicines and Healthcare products Regulatory Agency showed that the CPT Hip System has a fracture rate of approximately 1.4%.
However, similar devices typically have much lower fracture rates, ranging from about 0.6% to 1%. This higher fracture rate means that patients with the CPT Hip System are more likely to suffer from these painful and disruptive fractures compared to those with other devices.
It’s unacceptable that a device meant to improve quality of life is instead putting patients at higher risk of additional injury.
Imagine regaining the ability to walk without pain, participate in activities you love, or simply enjoy your daily life, only to have that ripped away from you because of a faulty medical device.
If you have suffered a femoral fracture because of a Zimmer Biomet hip replacement device, reach out to the Meshbesher & Spence legal team today online or by calling (612) 339-9121. You may qualify for financial support to assist you in your recovery.
FDA Recommendations for Patients and Doctors
The FDA has important recommendations for anyone with the Zimmer Biomet CPT Hip System:
- Discuss the benefits and risks of all hip replacement devices with your healthcare provider.
- If you experience unexpected pain or difficulty walking, consult your doctor right away.
- If you don’t have any unusual symptoms, continue with your regular follow-up appointments. The FDA does not recommend removing a well-functioning CPT Hip System.
Meanwhile, the agency advised doctors to:
- Go over these recommendations with patients.
- Use different hip replacement options when possible.
- Make patients aware of the risks if they have no other choice than the CPT Hip System.
The FDA stated that it is working closely with Zimmer Biomet to ensure everyone knows about the risks and is continuing to monitor the device’s performance. It will continue to provide updates and share any new information as it becomes available.
Do I Qualify for a Zimmer Biomet Hip System Lawsuit?
An experienced medical device lawyer can determine if you qualify for a claim. To be eligible for a case, you must have:
- Been implanted with a Zimmer Biomet CPT Hip System Femoral Stem 12/14 Neck Taper (CPT Hip System).
- Experienced a thigh bone fracture after surgery (postoperative periprosthetic femoral fracture).
In some cases, if you need revision surgery within a certain time, you may be able to file a claim. Your lawyer can help you understand whether you are eligible and when the deadlines are for a Zimmer Biomet hip system lawsuit.
Other Lawsuits Against Zimmer Biomet
This isn’t the first time the safety of Zimmer Biomet products has been called into question.
The medical device manufacturer has faced hundreds of other lawsuits over allegedly harmful products, such as its M/L Taper hip implant, VerSys metal femoral head, M2a Magnum devices, Durom Cup implants, and knee replacement devices.
Meshbesher & Spence: Trusted Medical Device Lawyers
When people get a medical device, they trust it has been tested and is safe to use. It’s natural to expect these devices will work as intended without causing complications.
We understand that it’s extremely frightening to learn that something implanted inside your body could be compromised.
If you’ve suffered a fracture from the CPT Hip Replacement System, you don’t have to face this alone. Our lawyers have successfully supported people through countless claims involving defective medical devices. Get in touch with us online or call (612) 339-9121.
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