Stryker knee replacement recall 2017

Stryker Corp. This implant, which is used exclusively with Stryker ShapeMatch Cutting Guideshas been linked to complications including joint instability or looseness, fracture, chronic pain, reduced mobility, and hip replacement failure.

Free Confidential Lawsuit Evaluation: If you or a loved one had complications after knee replacement surgery, you should contact our law firm immediately.

You may be entitled to compensation by filing a suit and our lawyers can help. The Stryker Triathlon knee was approved by the U. The implant combines hi-tech materials and equipment that are supposed to provide improved post-surgical results over earlier models, according to Stryker.

However, despite these features, the Stryker Triathlon knee has been linked to reports of adverse health complications in patients who received the device. The recall was initiated after Stryker received at least 44 reports of inaccurate bone cuts resulting in hip replacement complications.

Class I recalls involve products or devices which can cause adverse health consequences or death, according to the FDA. When surgeons use incorrect ShapeMatch Cutting Guides with Stryker Triathlon knee implants, it may cause the following complications:. The Medical Device Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in Stryker Triathlon Knee Lawsuits.

We are handling individual litigation nationwide and currently accepting new knee replacement injury cases in all 50 states. Free Case Evaluation: Again, if you had problems with a knee implant, you should contact our law firm immediately. You may be entitled to a settlement by filing a suit and we can help.

stryker knee replacement recall 2017

Medical Devices. Share on Facebook Share on Twitter.If you had a bad knee replacement or needed surgery, you should contact our lawyers immediately for a free case consultation.

Please use the form below to contact our Defective Medical Device Litigation Group or call us toll-free 24 hours a day at In Octobera man who had an allergic reaction to cobalt and nickel in the Stryker Triathlon knee replacement has filed a lawsuit PDF in Colorado. Click here to read more. The recall was issued because software defects may result in inaccurate bone cuts, a poorly-fitting implant, loose or unstable knees, severe pain, and other injuries that require revision surgery.

At least 44 incidents were reported to the FDA. This guide is used before and during surgery. Then, the surgeon uses the ShapeMatch Cutting Guide to choose the most appropriate components of the Triathlon knee. Accuracy is extremely important during this procedure. The problem with the Stryker Triathlon knee implant is that software defects in the ShapeMatch Cutting Guide may result in improper bone cuts and a poorly-fitting knee implant.

Stryker Must Pay $7.6M for Defective Knee Replacements

In the recall notice, the FDA warned:. Additionally, Stryker Orthopaedics determined that another software defect resulted in the displayed parameters e. This may result in serious adverse health consequences including joint instability, fracture, need for revision surgery and chronic pain and limitations of mobility. The Stryker Triathlon has not been recalled.

However, a surgical instrument that was used to implant the Stryker Triathlon has been recalled. If you had knee surgery and you are now suffering from pain, looseness, limited mobility, or required revision surgery for your knee implant, you may qualify for a lawsuit. There are at least 44 reports of incidents and injuries associated with the Stryker Triathlon knee implant in which the ShapeMatch Cutting Guide was used.

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What is the Stryker Triathlon Knee? What is the ShapeMatch Cutting Guide?

Problem with the Stryker Triathlon Knee Implant The problem with the Stryker Triathlon knee implant is that software defects in the ShapeMatch Cutting Guide may result in improper bone cuts and a poorly-fitting knee implant.

How Many Incidents Were Reported? Search the Site Search for:.In other words, 5 percent of all people over the age of 50 have had one knee replaced. And that number keeps growing: over the last decade, the number of knee replacements has doubled.

In alone,knee replacement surgeries were performed in the United States. Unfortunately, not all knee surgeries go as planned. Though most patients reported reduced pain and increased mobility, an unfortunate few experience very severe complicationslike chronic pain, infection, and reduced range of motion.

Some fall prey to device failure and must have early revision surgery. And for many, these problems are later explained by a knee replacement recall. In the last five years, artificial knee recipients have been hit by a major Stryker knee recall and a Zimmer knee recall. Thousands have been affected. The U. The FDA is responsible for many aspects of device approval and ongoing safety, including initial device clearance and any eventual recalls.

The FDA has a big job: U. For this reason, the federal agency takes certain measures to streamline its medical device approval process. This fast track approach may make for speedy approvals, but many medical professionals, politicians and consumers know it can also pave the way for serious knee replacement complications.

When a device qualifies for premarket approval, the manufacturer is legally allowed to bypass premarket testing and other safety measures. The biggest problem is that when the previously approved device is unsafe or recalled, the new device can remain on the market.

Over the last decade, the FDA has received many adverse even reports for knee replacement systems and components.

Persona Knee: Loosening & Failure lead to Zimmer Recall

To date, DePuy has issued several important recalls for its knee replacement devices. For most U. The device was pulled off the market after a manufacturing substance had lodged in patient joint surfaces, resulting in painful swelling.Although every patient recovers differently, here are some of the things you may expect in the days, weeks, and months following knee replacement surgery.

Knee Replacement Recall

Your orthopaedic surgeon, nurses, and physical therapists will closely monitor your recovery progress. Most knee replacement patients are encouraged to walk with assistance, such as a cane, walker, or crutches, on a level surface and climb up and down two or three stairs within one to four days after surgery or before discharge from the hospital. Initially, activity will cause discomfort, so your care team may recommend pain medication prior to physical therapy.

Gradually, your pain medication will be reduced, the IV will be removed, your diet will progress to solids, and you will become increasingly mobile. Your physical therapist will talk with you about how to continue your progress after your hospital stay. They will also go over exercises to help improve your mobility. An occupational therapist may show you how to best perform daily activities, such as putting on socks, reaching for household items, and bathing.

A case manager will discuss plans for your return home to help ensure you have all the necessary support for your recovery. Using a cane or walker may be necessary for several weeks. Ask your doctor about any unusual symptoms that you should look out for after surgery.

Stryker Reaches New Settlement Agreement in Wake of Falling Revenues

This may include, but is not limited to, pain in your leg unrelated to your incision, persistent fever, severe swelling, or drainage from the wound. Movement is essential to a healthy recovery. Recommended activities include gradually increased walking and light household activities, such as climbing stairs. After the initial recovery from surgery, most people can resume normal routine activities within the first 3 to 6 weeks of their total knee replacement.

Also, athletic activities that place excessive stress on the replaced joint, such as basketball, distance running, contact sports or frequent jumping, should be avoided.

Your doctor will work with you to determine the most appropriate level of activity for you. Total knee replacement is intended for use in individuals with joint disease resulting from degenerative, rheumatoid and post-traumatic arthritis, and for moderate deformity of the knee. Knee replacement surgery is not appropriate for patients with certain types of infections, any mental or neuromuscular disorder which would create an unacceptable risk of prosthesis instability, prosthesis fixation failure or complications in postoperative care, compromised bone stock, skeletal immaturity, severe instability of the knee, or excessive body weight.

As with any surgery, knee replacement surgery has serious risks which include, but are not limited to, pain, infection, bone fracture, peripheral neuropathies nerve damagecirculatory compromise including deep vein thrombosis blood clots in the legsgenitourinary disorders including kidney failuregastrointestinal disorders including paralytic ileus loss of intestinal digestive movementvascular disorders including thrombus blood clotsblood loss, or changes in blood pressure or heart rhythmbronchopulmonary disorders including emboli, stroke or pneumoniaheart attack, and death.

Knee implants may not provide the same feel or performance characteristics experienced with a normal healthy joint. The information presented is for educational purposes only.

Speak to your doctor to decide if joint replacement surgery is right for you. Individual results vary and not all patients will return to the same postoperative activity level. The lifetime of any joint replacement is limited and varies with each individual. Your doctor will counsel you about how to best maintain your activities in order to potentially prolong the lifetime of the device.

Such strategies include not engaging in high-impact activities, such as running, as well as maintaining a healthy weight. Ask your doctor if the joint replacement is right for you. Stryker Corporation or its other divisions or other corporate affiliated entities own, use or have applied for the following trademarks or service marks: Mako, Mobile Bearing Hip, Stryker, Together with our customers, we are driven to make healthcare better.

All other trademarks are trademarks of their respective owners or holders. Our website was designed for a range of browsers. However, if you would like to use many of our latest and greatest features, please upgrade to a modern, fully supported browser. Note: If you are browsing in Internet Explorer 9 or later, and you are still seeing this message, you may be in Compatability Mode.More accurate bone removal and implant placement, which may result in improved outcomes and functioning of the knee.

Quicker recovery, where 9 out of 10 patients were walking without an aid, such as a cane or walker, three weeks after surgery. Prior to surgery, a CT scan of your knee joint is taken in order to generate a 3D virtual model of your unique anatomy. This additional information helps your doctor determine the optimal size, placement and positioning of your implant.

Throughout your procedure, Mako provides real-time data to your surgeon. This allows them to continuously assess the movement and tension of your new joint, and adjust your surgical plan if desired. In the operating room, the surgeon guides the robotic-arm to remove the arthritic bone and cartilage from your knee. The Mako System creates a virtual boundary that provides tactile resistance to help your doctor stay within the boundaries defined during the planning process.

With the diseased bone gone, your implant is placed into the knee joint. Severe knee pain or stiffness resulting from: noninflammatory degenerative joint disease including osteoarthritis, traumatic arthritis, or avascular necrosisrheumatoid arthritis or post-traumatic arthritis. Partial knee replacement is intended for use in individuals with joint disease resulting from degenerative and post-traumatic arthritis, and for moderate deformity of the knee.

Partial knee replacement surgery is not appropriate for patients with certain types of infections, any mental or neuromuscular disorder which would create an unacceptable risk of prosthesis instability, prosthesis fixation failure or complications in postoperative care, compromised bone stock, skeletal immaturity, severe instability of the knee, or excessive body weight.

As with any surgery, knee replacement surgery has serious risks which include, but are not limited to, pain, infection, bone fracture, peripheral neuropathies nerve damagecirculatory compromise including deep vein thrombosis blood clots in the legsgenitourinary disorders including kidney failuregastrointestinal disorders including paralytic ileus loss of intestinal digestive movementvascular disorders including thrombus blood clotsblood loss, or changes in blood pressure or heart rhythmbronchopulmonary disorders including emboli, stroke or pneumoniaheart attack, and death.

Partial knee implants may not provide the same feel or performance characteristics experienced with a normal healthy joint. The information presented is for educational purposes only.

Speak to your doctor to decide if joint replacement surgery is right for you. Individual results vary and not all patients will return to the same postoperative activity level. The lifetime of any joint replacement is limited and varies with each individual. Your doctor will counsel you about how to best maintain your activities in order to potentially prolong the lifetime of the device.

Such strategies include not engaging in high-impact activities, such as running, as well as maintaining a healthy weight. Ask your doctor if Robotic-Arm Assisted Surgery is right for you. Stryker Corporation or its other divisions or other corporate affiliated entities own, use or have applied for the following trademarks or service marks: Mako, Mobile Bearing Hip, Stryker, Together with our customers, we are driven to make healthcare better.

All other trademarks are trademarks of their respective owners or holders. Our website was designed for a range of browsers.

stryker knee replacement recall 2017

However, if you would like to use many of our latest and greatest features, please upgrade to a modern, fully supported browser. Note: If you are browsing in Internet Explorer 9 or later, and you are still seeing this message, you may be in Compatability Mode.

We use cookies to customize content for your viewing and for analytics. If you continue to browse this website, we will assume that you are happy to receive all our cookies. For further information please read our cookie policy. Knee Knee About knee pain. Hip About hip pain.

Top Stryker Competitors in the United States

Foot About foot pain. Ankle About ankle pain.Do you have a defective knee that needs to be replaced or revised? Do you know why it failed? Do you know what device the surgeon is suggesting to do the repair with? Are you aware of what the success or failure rates of the revision components? Our firm has reviewed thousands of examples of prosthetic failures and can help you get answers.

Revision surgery for the replacement of an initial index implanted knee due to premature failure is unfortunately all too common. Often times there is systemic inflammation from various materials including titanium TICobalt- Chrome CO-CR various polymers, ceramics that result in frictional wear, metallosis or galvanic corrosion that is gradual or leads to a sudden mechanical failure.

The patient rarely picks the component or the manufacturer. How do you know what is going to be used before it is implanted? Simple, Just ask. More than different knee replacement devices are available from a variety of manufacturersincluding:. To research a failed implant or to find out if there are problems with the device you are being revised to, go to the FDA database for information on whether the products have a reported history of failing and why.

stryker knee replacement recall 2017

A knee replacement system consists of two main components — a tibial trey and a femoral implanted component. The weight of the patient is transferred between these two components, allowing for activity and motion. The joint is typically constructed with a surface of plastic or polyethylene construct, sometimes in a single piece or in a modular construct involving multiple, interchangeable pieces.

When these devices fail because of component loosening or premature wear, this failure can necessitate an additional surgical procedure. A claim against the device manufacturer can allow you to recover for these additional damages, which are often substantial. Your email address will not be published.

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We offer market-leading knee replacement implants for partial knee and total knee arthroplasty for primary and revision procedures featuring our cemented and cementless flagship TKA solution, the Triathlon Knee System. Knee Implants We offer market-leading knee replacement implants for partial knee and total knee arthroplasty for primary and revision procedures featuring our cemented and cementless flagship TKA solution, the Triathlon Knee System.

Designed to work with the body Our Triathlon Total Knee System portfolio offers you many options to treat patients needing a total knee replacement. Since its launch inmore than 2 million patients have received a Triathlon knee. The Triathlon single radius has been designed to work with the body to promote a natural-like circular motion, to help restore function and relieve pain.

stryker knee replacement recall 2017

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