Pittsburgh Zimmer NexGen Knee Replacement Injury Lawyers from the Pennsylvania-based law firm have argued for their plaintiffs that the implant surgery where this device was used had completely failed caused by the malfunction of the NexGen MIS device. With the growing number of revision surgeries among patients, the US Food and Drug Administration issued a recall notice to Zimmer Holdings Inc. to withdraw the faulty knee replacement device from the market. In September, 2010, the FDA categorized this as a Class II action as a response to nearly 114 MDRs or medical device reportings.

What is NexGen MIS Device Used For?

Zimmer manufactured a series of knee replacement products to be included in the NexGen series of devices. Three such examples are NexGen CR-Flex, NexGen LPS-Flex and NexGen MIS Tibial Component. The MIS Tibial component is supposed to replace an individual’s tibia or the shinbone. Two bones stretch from the ankle to the knee known as fibula and tibia respectively. It is the latter one that is the larger of the two and is responsible greatly for an individual’s movements and mobility. The NexGen MIS Tibial device is implanted in the patient during the knee replacement surgery through a small incision. The structure of this component is such that it was easier both for the surgeon and the patient to tackle with it.

What Are the Issues With the NexGen MIS Device?

Zimmer’s NexGen MIS Tibial device was deemed defective by medical professionals because it showed signs of premature loosening and subsequently painful revision surgeries. Clients of the Pittsburgh Zimmer NexGen Knee Replacement injury lawyers have claimed that faced the following complications after receiving knee replacement surgery where the NexGen MIS device was used:

• Severe infections
• Additional loss of bone
• Untimely and urgent revision surgery
• Dislocation (the device does not lock properly after implant)
• Swelling and inflammation at the site of surgery
• Distinguishable warmth at the joint
• Instability
• Shooting pain along the leg where replacement surgery took place

If you have faced any of the listed complications, you might be entitled to a financial compensation. Contact the Pittsburgh injury lawyers at the Logue Law Group for details on the procedure.

When medical authorities were questioned about the possible side effects of a poorly executed knee replacement surgery, they asserted that:

• It can cause serious difficulty in standing up and walking around by oneself
• Loosening of the NexGen MIS Tibial component can cause the device to slip out of the socket

Who Needs NexGen MIS solution?

Medical representatives have explained that the following individuals are likely to have been implanted with NexGen MIS knee replacement component:

• Extreme knee pain
• Disability in movement
• Rheumatoid arthritis
• Traumatic arthritis
• Osteoarthritis
• Polyarthritis

What Should You Do?

Zimmer Holdings Inc. is currently facing nearly 1300 lawsuits with regards to premature failing of knee replacement surgeries. It was reported that approximately 68,383 devices have already been implanted into patients across the country. The US FDA received no less than 114 official complaints concerning the NexGen MIS knee replacement devices. If you or someone you know has undergone replacement surgery where Zimmer NexGen MIS devices were used, you should contact the Pittsburgh injury lawyers to evaluate your case for a free and non-obligatory, private consultation. Our lawyers at the Logue Law Group have the reputation of providing impartial and exclusive attention to each client.

What is Zimmer Durom Acetabular Cup Used For?

The traditional hip replacement surgeries involved plastic or ceramic devices that would fit in the hip socket and facilitate movement for the patients. The Durom Cup by Zimmer Holdings Inc. has a metal-on-metal bearing which was designed to cause low friction and lower wear and tear. The Durom Acetabular component perfectly partners with the Durom femoral component, making movement and recovery extremely easy for the patients undergoing replacement surgery. Logue Law Group has heard from a lot of clients that the Durom Cup made promising advertisements and was considered one of the best hip replacement prosthesis devices.

What Do We Know About the Zimmer Durom Hip Recall Lawsuit?

The Durom Cup by Zimmer was available for only a short period of two years, till it was recalled in July, 2008. Pittsburgh Zimmer Durom hip injury lawyers asserted as representatives of the plaintiff that the orthopedic device failed to mate with the host bone, which is the basis of any hip replacement surgery. Owing to this malfunction, the Durom Cup freely migrates from its designated position, causing severe damage to the patient’s body. Logue Law Group consulted with the medical authorities and found that most of the patients who were implanted with the Durom Cup during the hip replacement surgery had undergone a revision surgery to rectify the issues caused by this faulty medical device. Pittsburgh injury lawyers argued on behalf of the plaintiffs that the rate of revision surgeries in case of Durom Cup was significantly higher than the traditional replacement devices. The Zimmer Durom recall lawsuit claims that this device was designed to increase the flexibility and life-span of artificial hips, which it utterly failed in doing.

What Are the Main Issues of the Durom Cup?

As several patients were suffering from severe side effects of the Durom Cup, the US FDA urged medical authorities to point to the main issues with this device. Dr. Lawrence Dorr, a notable orthopedic surgeon from Los Angeles, wrote in a letter to the American Association of Hip and Knee Surgeons that:

• The patients with the Durom Cuo showed all the symptoms of a loose hip implant, even though X-rays might not point to it.
• The dimeter and the surface of fixation of the Durom Cup was not adequate.
• The techniques used by the surgeons to implant the faulty device was not an issue, even though the manufacturers constantly held on to this statement.

Nearly twelve thousand patients had been implanted by the Durom Cup in the US and most of them had to undergo correctional surgeries.

What Should You Do?

If you had undergone a hip replacement surgery where the Durom Cup was used, you might be entitled to a pecuniary compensation. You should contact the Logue Law Group in Pennsylvania and get in touch with the Pittsburgh injury lawyers for a free evaluation. These compensations are rewarded to:

• People who had to undergo a revision surgery within 180 days of being implanted with the Durom Cup
• People who passed away after filing an official complaint

Reach out to us and get a free case evaluation along with the best legal advice. Our lawyers will ensure you get compensated for the pain you had to suffer through.

The Pittsburgh Zimmer Biomet Reverse Shoulder lawsuit lawyers from the Logue Law Group argued for the plaintiffs that the manufacturers were well aware of the potential malfunctioning properties of these devices, yet marketed them actively. Their negligence had caused the suffering of thousands of patients. This could have been easily prevented had Zimmer Biomet informed medical authorities and the US FDA about this grave issue.

What is the Use of Reverse Should System?

The Reverse Should System is an implantable medical tool for the Comprehensive line of medical devices by Zimmer Biomet. This is generally used by surgeons for patients who had:

• Deficient rotator cuff and rotator cuff tears
• Shoulder arthritis or arthropathy
• Previous failures of shoulder joint replacement surgeries
• Failed in responding to traditional shoulder joint replacement surgeries

The Comprehensive Reverse Shoulder System is used for restoring the arm movement among patients who suffered from the listed ailments. This medical device is surgically implanted into the patients and its function is to be anatomically opposite to the conventional shoulder replacement devices. It is designed to work contrary to an individual’s natural shoulder anatomy. The manufacturers claimed that this apparently works better for patients who are suffering from arthropathy and other shoulder ailments. Pittsburgh Zimmer Biomet Reverse Shoulder lawyers conferred with medical professionals and found out that this device does not rely on the rotator cuff, but on the deltoid muscle. This supposedly helps stabilize the arm and facilitate movement as well as recovery sooner.

What is the Zimmer Biomet Shoulder Replacement Lawsuit?

Despite the active marketing strategies, the acute design flaw of the Comprehensive Reverse Shoulder System led to thousands of implant failures. This prompted Zimmer Biomet to voluntarily recall this faulty medical device from the market on December 15, 2016. They sent an Urgent MDR Notice (Medical Device Recall) to all healthcare institutions that were using the Comprehensive Reverse Shoulder System for replacement surgeries. The Pittsburgh Zimmer Biomet Reverse Shoulder lawsuit lawyers asserted as plaintiff representatives that this faulty device has led a number of painful revision surgeries among patients across the country. Later, the FDA identified this as Class I recall, which points to the fact that it can cause irreversible injuries and even death.

What are the Complications After Using Reverse Shoulder Implant Device?

The Pittsburgh Zimmer Biomet Reverse Shoulder lawyers learnt after consulting with healthcare experts that there are a series of side effects linked to this implantable replacement device. Since most patients required immediate revision surgeries, they were under the risk of undergoing the following complications:

• Severe infections
• Bone damage
• Tissue damage
• Extreme pain
• Disability in shoulder movement
• Permanently losing shoulder movement
• Death

If you have experienced any of these side effects after being implanted with the Comprehensive Reverse Shoulder System, you must consult with your medical representative and contact the Pittsburgh injury lawyers at the Logue Law Group.

What Should You Do?

There were nearly 3,662 Comprehensive Reverse Shoulder Humeral Trays that were distributed over the eight years of production. Most of them have been used in surgeries and the patients had to suffer through another surgery to correct the malfunction caused by it. If you or someone you love has been affected by this faulty implantable replacement device, you should immediately reach out to the Pittsburgh personal injury lawyers to evaluate your case. You might be entitled to monetary compensation for any loss of wage, medical expenditure and some other punitive damages. Our lawyers at the Logue Law Group will guide you and give you the best legal advice.

Logue Law Group has helped several clients file lawsuits who claimed to have suffered through the painful side effects of the pelvic mesh. Pittsburgh transvaginal mesh lawsuits alleged that these medical devices have the potential to induce aching, bleeding, vaginal infections, perforation of other organs and autoimmune difficulties. The numerous side effects of the transvaginal mesh and thousands of lawsuits being filed against the leading manufacturers of the medical device necessitated some urgent actions. This led to the US Food and Drug Administration (FDA) to issue recall warnings to the manufacturers of the transvaginal mesh devices.

What is the Vaginal Mesh Used For?

Clients of the Pittsburgh transvaginal mesh lawsuit lawyers asserted that this medical device is used to help women who are suffering from gynae issues like pelvic organ prolapse and stress urinary incontinence. POP is the condition where the muscles which hold the pelvic organs in their place are gradually weakened and cannot serve their purpose anymore. This can result in the bladder getting dropped or prolapsed which presses against the vaginal walls. Whereas, SUI is when activities such as sneezing or coughing lead to urine leakage through the urethra. The transvaginal mesh is made of synthetic porous materials which provide support to the weakened tissues and repair the damaged ones. This medical device has been used to treat SUI since the 1990s whereas it was not until 2002 that they were used for pelvic organ prolapse treatment. It is surgically implanted into patients and the central function of this device is to create stability again.

What is the Issue with the Vaginal Mesh?

The transvaginal mesh is made up of synthetic materials which help women through their gynae issues. These materials often have edges which have the possibility of tearing tissues and perforate other surrounding organs. It can also puncture the abdominal region, uterus and the bladder causing severe side effects in the individual who is implanted with it. Pittsburgh injury lawyers from the Logue Law Group have argued on behalf of the plaintiffs that this bladder sling can move around in the patient’s body, giving rise to irreparable issues and horrible vaginal infections.

What is the Transvaginal Mesh Lawsuit?

The FDA had issues heightened warnings in July, 2011 against the use of vaginal mesh for treatment of POP. With thousands of complaints and cases being filed against the manufacturers, the FDA three months later in September, 2011 reclassified these medical devices to cease their 510(k) clearance. Pittsburgh transvaginal mesh lawsuits have mostly been filed against the following-

• Gynemesh, Ethicon (manufactured by Johnson & Johnson)
• Pelvisoft, Avaulta (manufactured by C.R. Bard)
• Perfyx, Obtryx, Pinnacle (manufactured by Boston Scientific)
• Spar, Perigee, Monarc (manufactured by American Medical Systems)

Pittsburgh Transvaginal Mesh Lawsuit Lawyershave argued as representatives of the plaintiff that these medical devices have the high-risk factors of erosion, constant need to repair and failure.What Should You Do?

If you have been surgically implanted with the transvaginal mesh, you need to check with your healthcare professional whether you have any of the following issues:

• Organ damage
• Mesh erosion
• Mesh sticking to the vagina or bladder
• Vaginal scarring
• Dyspareunia (pain during intercourse)
• Uterine prolapse
• Urinary disfunction

In case you have developed any of these symptoms or suffered through acute pain after your implant surgery, you should contact the Pittsburgh injury lawyers. They will provide with private consultations and fight for the due compensation that you might be eligible for.

If you or your loved one has been a victim of addiction-related injuries, happening from JUUL e-cigarette, then you need to file a claim for compensation. The manufacturer company JUUL has been charged for deceptively marketing their e-cigarettes and thus made a whole generation of young adult people addicted to highly concentrated nicotine delivery system. So, if you or your loved ones have been exposed to the risk of consuming highly concentrated nicotine, then you need to immediately seek help from Pittsburgh JUUL lawyer. At Logue Law Group, our team is ready and has enough experience to handle your case of JUUL lawsuits.Things You Need to Know About JUUL Vaping Lawsuits

Electronic cigarettes or popularly known as e-cigarettes are a very famous product amongst the young adults of the country. Shaped like a cigarette, pen, or USB flash drive, this contains liquid nicotine in various flavors along with propylene glycol and glycerin. Heated by a battery and heating coil, this liquid produces vapor because of which “vaping” is a popular term for the people who are addicted to this.

The high amount of nicotine that is used in JUUL products makes the user easily addicted. One JUUL pod contains the same amount of nicotine as a whole pack of cigarettes and as it remains concentrated, it gets absorbed by the body more quickly than the traditional cigarettes.

The government agencies have charged JUUL for deceptive marketing of the products using different flavors like mint, fruit, crème, and so on and making a whole new generation addicted to the product. They relied on social media more for marketing their e-cigarettes which became hugely popular since the time the company started manufacturing it. The aggressive advertising and glamorizing vaping since 2017 have made many teenagers addicted to it. Studies show that the 12th-grade students reported for smoking were only 3.6% in 2018 whereas 3.6 million middle and high school students are found to addicted to vaping. If your loved one has been an addict too, then come to us and consult our Pittsburgh JUUL lawyer to file your claim for compensation.JUUL Injuries and Side Effects

Vaping JUUL e-cigarettes not only expose the user to excessive nicotine addiction but also some more serious health issues. The FDA has received many reports of teenagers and young adults suffering from convulsions and seizures due to nicotine poisoning and toxicity.

Symptoms of Nicotine Poisoning are:

• Convulsions
• Embolism
• Blood clotting
• High blood pressure
• Injuries in heart
• Pain in the joints
• Strokes
• Seizures

Apart from that, the chemicals used in vape juice for flavoring the vapor include diacetyl, formaldehyde, toluene, and acrolein. These chemicals can the development of bronchiolitis obliterans which causes permanent damage in the lungs called “popcorn lungs.”

If you or your loved one is already seeing these symptoms and experiencing more difficulties, then you need to talk to the physicians right away. Also, make sure that you are getting in touch with an experienced Pittsburgh JUUL lawyer who can help you with the legal proceedings of the claim.Compensation You Will Get From JUUL Lawsuit

If you or your loved one is affected by the JUUL e-cigarette, then you can file the claim seeking the following damages that Pittsburgh injury lawyer will help you with:

• Medical expenses that cover the treatment of injuries as well as addiction
• Damage for physical pain and suffering caused by the addiction-related injury, the trauma, and the complex treatment and recovery process
• Loss of life quality
• Punitive damages if it is applicable

Seek Help From Pittsburgh Addiction Injury Lawyer

At Logue Law Group, we have our team of seasoned lawyers who are not only capable but also have a history of dealing with the cases of JUUL lawsuits. So, if you are looking for Pittsburgh JUUL lawyer to hear about your claim, call us right away.

The inferior vena cava (IVC) filter is a medical device that is used to prevent blood clots and is implanted by experienced vascular surgeons. While this was supposed to prevent embolisms and unforeseen lumping of blood, the faulty nature of the IVC filters was intentionally concealed by the manufacturers. The lawsuit that ensued claims that the malfunctioning IVC filters have resulted in a high rate of injuries among the patients who were implanted with this device.What is the IVC Filter Lawsuit?

As these IVC filters turned out to be flawed, unmediated panic arose in the medical world. Patients were reported to be experience internal bleeding, excruciating pain and some instances of damage to organs were also found. Pittsburg product liability lawyers have argued that the manufacturers of this faulty medical tool did not warn the distributors, doctors, surgeons or patients about the higher risk rates of using the IVC filter. The lawsuit describes that the filter breaks after being surgically inserted inside patients. This resulted in the metal bits found in the IVC filter to move along the blood flow of the body, whereby increasing the risk of organ damage and internal bleeding. The Pittsburg IVC filter lawyers are accepting clients who had undergone this surgery and have faced any of the adverse effects.

Pittsburg IVC filter lawyers have also argued that the manufacturer of the medical device, C.R. Bard had hidden the correct results which proved the dangerous nature of the filter. The lawsuit also states that in order to obtain Food and Drug Administration (FDA) approval, the manufacturer had forged the signature of an employee on the application form.What are the Injuries and Side Effects of the IVC Filter?

Several instances of the IVC filter breaking and falling out have been reported by patients. The metal fragments can easily be set in motion through the blood stream and puncture veins or inflict serious injury to organs. The Pittsburg IVC filter lawyers have argued that there have been ironic cases of blood getting clotted in the very place this filter was inserted to prevent the clot. Following is list of common as well as severe injuries that can be caused by the IVC filter. In case you believe that you have faced any of this due to your IVC filter, seek immediate medical care from healthcare professionals.Common Injuries Caused by IVC Filters

• Sudden pain in chest
• Confusion
• Irregular heartbeats
• Hypotension
• Nausea
• Breathlessness
• Dizziness
• Internal bleeding
• Neck Pain

Extreme Injuries Caused by IVC Filters

• Pulmonary embolism
• Stroke
• Hemorrhage
• Death

What is the Compensation in the IVC Filter Lawsuit?

If you have suffered through any of the injuries caused by the IVC filter, the Pittsburg product liability lawyers will seek the following compensations for you:

• Any medical expenditure incurred due to the IVC filter, both past and future.
• The mental and physical pain caused by the filter along with the expenditure on the treatment process.
• Any loss of wage or the ability to earn a livelihood in the past or the future because of the IVC filter.
• The loss of recreation and relaxation in life due to the IVC filter.
• Other punitive injuries if considered appropriate will also be covered as compensation

This medical tool was designed to ease the pain of ailing patients and it ended up causing more damage to them than they initially had. The Pittsburg IVC filter lawsuit lawyers argue that this device is likely to perforate or fracture the inferior vena cava which is the largest vein found in the body. Not less than ten thousand lawsuits have been filed against the manufacturers of this defective filter in the federal court by patients who claim to have faced the minor and major damages caused by it.

If you have undergone the surgery for IVC filters and experienced any of these injuries, reach out to the Logue Law Group. Contact us today and get the best possible compensation for the pain you suffered through.