#Transvaginal Mesh Implant

[unwelcome-ozian]

What information do you have about Johnson & Johnson?

Alza filed an NDA for the transdermal opioid analgesic product in December 1987 for post-operative use and for the relief of chronic cancer pain. Developed by J&J subsidiary Janssen Pharmaceutica, fentanyl has been marketed since 1968 under the Sublimaze brand. The drug is currently approved for I.V. administration and used primarily as a short-acting analgesic during anaesthesia. "This new drug delivery system will make it possible for the first time to use fentanyl . . . outside the operating room to control moderate to severe pain." Source

US opioids: Johnson and Johnson and drug distributors offer $26bn to end thousands of lawsuits. Source

The drug company Johnson & Johnson (J&J) has expressed regret after court documents unsealed in talcum powder litigation showed that it funded a 1971 study in which Pennsylvania prison inmates, most of them black, were injected subcutaneously with asbestos. Source

Asbestos Prisoner Study May Spell More Problems for Johnson & Johnson

WASHINGTON - Global health care giant Johnson & Johnson (J&J) and its subsidiaries will pay more than $2.2 billion to resolve criminal and civil liability arising from allegations relating to the prescription drugs Risperdal, Invega and Natrecor, including promotion for uses not approved as safe and effective by the Food and Drug Administration (FDA) and payment of kickbacks to physicians and to the nation’s largest long-term care pharmacy provider.  The global resolution is one of the largest health care fraud settlements in U.S. history, including criminal fines and forfeiture totaling $485 million and civil settlements with the federal government and states totaling $1.72 billion. Source

Johnson & Johnson paused all clinical trials of its experimental COVID-19 vaccine after a study participant became sick with an "unexplained illness."

Johnson & Johnson has suspended international trials of a drug in the same class as an experimental drug made by Portuguese pharmaceutical company Bial, whose tests in France left one person brain dead and five others hospitalised. Source

1982 - McNeil

Product Recalled - Tylenol (acetaminophen) capsules

Reason for Recall - Medicine laced with potassium cyanide (poison) resulting in several patient deaths.

2009 to 2011 - McNeil

Product Recalled - Several OTC medicines including Tylenol, Motrin, Benadryl, St. Joseph aspirin, Sudafed, Pepcid, Mylanta, Rolaids, Zyrtec, Zyrtec Eye Drops (tens of millions of bottles)

Reason for Recall - Unpleasant smells causing nausea; tiny metal shards in liquid medicines; wrong ingredient levels

2010 - DePuy [Pinnacle Systems]

Product Recalled - ASR Hip Resurfacing System and ASR XL Acetabular System (metal-on-metal hip implants)

Reason for Recall - Metal poisoning (metallosis); loosening of the implant or joint dislocation; additional surgeries

2012 - Ethicon

Product Recalled - Gynecare Prolift Kit, Gynecare Prolift+M Kit, Gynecare TVT Secure and Gynecare Prosima Pelvic Floor Repair System Kit (transvaginal mesh implants)

Reason for Recall - Perforation of organs; vaginal bleeding and scarring; mesh erosion; severe pain

2014 - Ethicon

Product Recalled - Power Morcellators

Reason for Recall - Spread of uterine cancer; rapid progression of the disease; death

2019 – Johnson & Johnson

Product Recalled – 33,000 bottles of Johnson’s Baby Powder

Reason for Recall – The FDA found a small amount of asbestos — a known carcinogen — in a sample

Xarelto

Number of Lawsuits - 13,511

Injuries - severe, sometimes deadly bleeding events, blood clots, wound leaks, infection

J&J was involved in seven of 2017’s top ten health-care-related verdicts.

The company was also involved in the third-largest pharmaceutical settlement with the U.S. Department of Justice. In 2013, J&J paid the Justice Department more than $2.2 billion. The settlement resolved civil and criminal allegations involving Risperdal, Invega and Natrecor.

May 2017

J&J paid $33 million to most U.S. states and the District of Columbia. The states charged J&J with misrepresenting the manufacturing practices behind certain drugs. This included its Motrin products. These products were later recalled.

Oz

[latestmarketresearchnews]

Medical Plastics Market Size, Share, Growth Analysis And Forecast Report 2030

The global medical plastics market was valued at approximately USD 52.9 billion in 2023 and is projected to experience a steady growth rate, with a compound annual growth rate (CAGR) of 7.4% expected between 2024 and 2030. The significant growth in this sector can be attributed to the advancements in the development of plastics and plastic composites used in medical applications, particularly in the production of essential components such as catheters, handles for surgical instruments, and syringes. A rising demand for sophisticated medical devices, especially for in-house use, is expected to drive the need for medical device packaging. Materials like polyethylene, polypropylene, and polycarbonate are becoming increasingly important in the manufacturing of medical devices. Additionally, the expansion of home healthcare owing to its cost-effectiveness compared to hospital-based or intensive care has fueled a greater need for various medical devices.

Demographic trends in the U.S. further support this market growth. According to the latest U.S. census, 16.8% of the U.S. population is aged 65 years and older, with the elderly population expected to reach 74 million by 2030. Notably, individuals over the age of 85 typically require the most intensive care, and this age group is expanding rapidly. In response to this growing need for elderly care, in March 2021, U.S. President Joe Biden proposed a significant investment of USD 400 billion over an eight-year period into Medicaid to support at-home care services for elderly and disabled individuals. This plan also aimed to increase the wages of caregivers. The rising costs and shrinking profit margins have put considerable pressure on healthcare providers and health insurance plans in the U.S., leading the government to implement crucial changes in healthcare funding and insurance coverage, including reforms introduced through the Affordable Care Act (ACA) and Medicaid.

Gather more insights about the market drivers, restrains and growth of the Medical Plastics Market

Product Segmentation Insights:

The Polyphenylsulfone (PPSU) resin segment led the medical plastics market in 2023, accounting for over 51% of the total revenue. This dominance is largely due to the material's excellent heat and chemical resistance, which makes it particularly suited for producing durable surgical tools and medical devices. PPSU's high strength and resilience make it a preferred material in the production of surgical robots and components used in biopharmaceutical processing. Additionally, its high flexural strength and impact resistance are beneficial for producing both single-use and multi-use surgical instruments, especially those that require repeated sterilization via steam.

Polyethylene (PE) is another important material in the medical plastics sector, valued for its resistance to bacteria and cleaning chemicals, making it ideal for use in medical equipment, devices, and other healthcare supplies. Its key characteristics such as impact resistance, chemical stability, flexibility, and minimal moisture absorption make PE suitable for use in medical-grade devices. Moreover, because it is a porous synthetic polymer that does not degrade within the human body, PE is used in various medical applications, including plastic surgery implants, tubing, and bottles.

Polypropylene (PP) is extensively used in the production of medical equipment and protective packaging, thanks to its toughness and durability. The strong chemical bonds of PP make it suitable for producing medical components like disposable syringes, connectors, finger-joint prostheses, non-absorbable sutures, reusable plastic containers, and laboratory items such as beakers and test tubes. Furthermore, PP is particularly beneficial in specialized medical procedures, such as hernia repairs and pelvic organ prolapse surgeries, where it is used in transvaginal mesh implants.

Order a free sample PDF of the Medical Plastics Market Intelligence Study, published by Grand View Research.

[alicesara611]

Key Players in the Pelvic Organ Prolapse Repair Device Market By 2024 to 2030

The global market for pelvic organ prolapse repair devices is poised to witness robust growth, projecting to reach a value of US$ 385.5 million by 2024 and expected to further increase to US$ 459.8 million by 2030. This growth is attributed to a Compound Annual Growth Rate (CAGR) of 3.2% from 2024 to 2030.

Pelvic organ prolapse (POP) is a prevalent medical condition where pelvic organs, including the uterus, bladder, and rectum, descend or sag into the vaginal cavity. Commonly caused by factors such as childbirth, aging, and weakening pelvic floor muscles, POP manifests with symptoms such as pain, discomfort, and urinary incontinence.

Discover Our Expert Analysis with Our Sample Report! https://absolutemarketresearch.com/Global-Pelvic-Organ-Prolapse-Repair-Device-Market/1157/request-sample

Several key factors contribute to the upward trajectory of the pelvic organ prolapse repair device market. The increasing prevalence of POP, a rise in the geriatric population, and a growing awareness of minimally invasive surgical procedures are identified as primary drivers propelling market expansion.

The demographic shift towards an aging population has significantly contributed to the rise in pelvic organ prolapse cases globally. As individuals age, the likelihood of experiencing weakened pelvic floor muscles and related conditions increases. This demographic trend, combined with an expanding awareness of minimally invasive surgical options, has fueled the demand for advanced and effective pelvic organ prolapse repair devices.

Minimally invasive procedures offer several advantages over traditional surgical methods, including reduced recovery times, lower risk of complications, and enhanced patient satisfaction. As awareness of these benefits continues to grow, the adoption of pelvic organ prolapse repair devices is anticipated to rise, further driving market growth.

Leading industry analysts predict that the market expansion will be sustained over the forecast period, creating opportunities for manufacturers, healthcare providers, and investors alike. The projected CAGR of 3.2% underscores the stability and potential profitability of the pelvic organ prolapse repair device market through 2030.

Companies operating in this space are encouraged to stay attuned to market trends, innovations, and evolving healthcare landscapes to capitalize on the opportunities presented by the growing demand for advanced pelvic organ prolapse repair solutions.

There are two main types of POP repair devices:

Transvaginal mesh: This is the most common type of POP repair device. It is a mesh implant that is inserted into the vagina and attached to the pelvic organs and surrounding tissues. The mesh provides support to the organs and helps to prevent them from prolapsing again.

Native tissue repair: This type of POP repair device does not use mesh. Instead, the surgeon uses sutures to repair and tighten the weakened muscles and tissues that support the pelvic organs.

The type of POP repair device that is right for you will depend on your individual circumstances and the severity of your prolapse. In some cases, a combination of a transvaginal mesh and native tissue repair may be used.

Benefits of POP Repair Devices:

Relieve symptoms of POP: POP can cause a variety of symptoms, such as urinary incontinence, bowel incontinence, and pain during intercourse. POP repair devices can help to relieve these symptoms.

Improve quality of life: POP can have a significant impact on a woman's quality of life. POP repair devices can help women to regain their independence and participate in activities that they may have had to avoid due to their prolapse.

Prevent further prolapse: POP can recur without treatment. POP repair devices can help to prevent further prolapse from occurring.

Regional Analysis:

North America is expected to hold the largest share of the global POP repair device market throughout the forecast period. This dominance is due to factors such as high prevalence of POP in North America, well-established healthcare infrastructure, and early adoption of new technologies.

Europe is expected to be the second-largest market for POP repair devices. The European market is driven by factors such as increasing awareness about POP, aging population, and growing demand for minimally invasive procedures.

The Asia Pacific market is expected to experience the fastest growth during the forecast period. This rapid growth is attributed to factors such as rising prevalence of POP in the region, increasing disposable incomes, and growing urbanization.

Key Players:

The global POP repair device market is characterized by the presence of a number of global and regional players. Some of the key players in the market include:

Boston Scientific Corporation

Johnson & Johnson/Ethicon

Medtronic plc

AMS/Uromed

Coloplast A/S

B. Braun Melsungen AG

Spacelabs Healthcare, Inc.

Bard Medical, Inc.

Cook Medical

Tensoplast

Segmentation:

The global POP repair device market can be segmented based on the following factors:

Product Type:

Transvaginal Tapes

Burch Colpocleisis

Sacrocolpopexy

Others

End-User:

Hospitals

Ambulatory Surgical Centers

Clinics

Geography:

North America

Europe

Asia Pacific

Latin America

Middle East and Africa

[garciaphan]

How Can A Defective Medical Device Lawyer Help Me?

If you or a loved one has been affected by a defective medical device, you may be wondering how a defective medical device lawyer can assist you. The answer depends on the particulars of your case, but a lawyer can explain your legal rights and options and, if necessary, represent you in court.

A defective medical device lawyer can assist you by investigating the facts of your case, collecting evidence, and conducting witness interviews. A lawyer can also help you understand how the law applies to your case and can negotiate on your behalf with the opposing party. A lawyer can represent you in court and help you fight for the compensation you deserve if your case goes to trial.

Contact a defective medical device lawyer immediately to discuss your options if you believe you may have a case against a medical device manufacturer. Continue reading to learn more about the topic.

What Is A Defective Medical Device?

A defective medical device is one that fails to meet the U.S. Food and Drug Administration’s safety or effectiveness standards (FDA). This includes hypodermic needles and pacemakers. If a medical device is found to be defective, the FDA will recall it and make it unavailable for use.

If a faulty medical device injured you, you may be able to file a claim against the manufacturer. These claims can be intricate, so it is essential to consult with an experienced defective medical device lawyer who can guide you through the legal process.

What Are Some Typical Examples Of Faulty Medical Devices?

Examples of typical faulty medical devices include:

Hip implants

Breast implants

Transvaginal mesh

Defibrillators

Pacemakers

Stents

What Compensation Am I Entitled To If A Defective Medical Device Caused My Injury?

If a defective medical device has injured you, you may be able to recover compensation for pain and suffering, medical expenses, and lost wages, among others. In some instances, you may also be able to recover punitive damages, which are intended to punish the negligent company.

Depending on the particulars of your case, the amount of compensation you may be able to recover will vary. If a faulty medical device has injured you, you should consult with an experienced defective medical device lawyer about your legal rights and available options.

How Can An Attorney For Defective Medical Devices Assist Me?

There are numerous types of faulty medical devices, including pacemakers and artificial hips. You may be entitled to compensation if a defective medical device has injured you. A defective medical device lawyer can assist you in filing a lawsuit against the device’s manufacturer and seeking compensation for your injuries.

It is essential to have an experienced attorney on your side when filing a lawsuit, as the procedure can be complicated. A defective medical device lawyer can assist you in gathering evidence, locating witnesses, and constructing a solid case against the manufacturer. If a faulty medical device injured you, contact an attorney immediately to discuss your legal options.

Conclusion

If you or a loved one has been injured by a defective medical device, you may be curious about how a defective medical device lawyer can assist you. The initial step involves contacting an attorney at Garcia and Phan. We will evaluate your claim and determine whether or not you have one. If you have a valid claim, we will assist you in filing a lawsuit and obtaining the appropriate compensation. Call us today at (714) 586-8298

[2hlawfirm]

How Can A Defective Medical Device Lawyer Help Me?

If you or a loved one has been affected by a defective medical device, you may be wondering how a defective medical device lawyer can help you. The answer depends on the specifics of your case, but a lawyer can help you understand your legal rights and options and can represent you in court if necessary.

A defective medical device lawyer can help you by investigating the facts of your case, gathering evidence, and interviewing witnesses. A lawyer can also help you understand the law and how it applies to your case and can negotiate with the other side on your behalf. If your case goes to trial, a lawyer can represent you in court and help you fight for the compensation you deserve.

If you think you may have a case against a medical device manufacturer, contact a defective medical device lawyer today to discuss your options. Keep on reading to find out more about the topic.

What is a defective medical device?

A defective medical device is any device that fails to meet the safety or effectiveness standards set by the U.S. Food and Drug Administration (FDA). This can include anything from hypodermic needles to pacemakers. If a medical device is found to be defective, it will be recalled by the FDA and will no longer be available for use.

If you have been injured by a defective medical device, you may be able to file a claim against the manufacturer. These claims can be complex, so it is important to speak with an experienced attorney who can help you navigate the legal process.

What are some common defective medical devices?

Some common defective medical devices include:

Hip implants

Breast implants

Transvaginal mesh

Defibrillators

Pacemakers

Stents

What compensation can I recover if I have been injured by a defective medical device?

If you have been injured by a defective medical device, you may be able to recover various types of compensation, including damages for your pain and suffering, medical expenses, and lost wages. In some cases, you may also be able to recover punitive damages, which are designed to punish the company for its negligence.

The amount of compensation you may be able to recover will depend on the specific facts of your case. If you have been injured by a defective medical device, you should speak with an experienced attorney to learn more about your legal rights and options.

How can a defective medical device lawyer help me?

There are many different types of defective medical devices, from pacemakers to artificial hips. If you have been injured by a defective medical device, you may be entitled to compensation. A defective medical device lawyer can help you file a lawsuit against the manufacturer of the device and seek damages for your injuries.

The process of filing a lawsuit can be complex, so it is important to have an experienced lawyer on your side. A lawyer can help you gather evidence, find witnesses, and build a strong case against the manufacturer. If you have been injured by a defective medical device, contact a lawyer today to discuss your legal options.

Contact a Defective Medical Device Lawyer At 2H Law

If you or a loved one has been harmed by a defective medical device, you may be wondering how a defective medical device lawyer can help you. The first step is to contact a lawyer 2H Law At  (619) 374-9320 . We will review your case and determine if you have a claim. If you do have a claim, we will help you file a lawsuit and get the compensation you deserve.

[spoonie-living]

WARNING: Lawsuits Against Multiple Boston Scientific Implants

Hey, friends, here’s a little PSA for folks with or considering any Boston Scientific implants: this company is sketchy as hell.

Spinal Cord Stimulator Devices

Concerns surrounding their spinal cord stimulator device are beginning to brew, with patients experiencing pain due to poor battery design and battery migration. You can read patient experiences in this thread on Patient.info, as well as this description of one patient’s pain and the cause of it on Avvo.com. Heads up that these links contain graphic descriptions of the effects and causes.

Boston Scientific is also facing whistleblower lawsuits surrounding various acts of fraud, including concealing defects and denying replacement devices.

Transvaginal Mesh & Slings

You may remember hearing about their transvaginal mesh devices, which caused terrible pain in many of their recipients and led to a whopping 48,000 lawsuits. This isn’t just one version of the device, either; there were lawsuits across multiple iterations, even after the recalls of their 1999 device.

Just a bad device? Seems like no: a recent 60 Minutes segment uncovered evidence suggesting they may have even knowingly used counterfeit plastic.

Bottom line? Don’t trust this company. If you’re looking at getting an implant from them, you may want to reconsider, or at least do your research to know what you’re getting into. And if you already have an implant, definitely look into your legal options and connect with affected patients. Solidarity is power 💜

You can find a little more info about the litigation against the company here [link contains diagrams of internal organs].

And thanks to @intentnevermakesasound for getting this on the ol' radar.

[abuselawyerca]

National Injury Help - Lawyers and Attorneys for defective products as well as drug side effects. Call (800) 214-1010 Free case reviews for any injury type.

[rapeculturerealities]

Hundreds of women living in pain after they were fitted with transvaginal mesh devices have won a landmark class action case against Ethicon, a subsidiary of Johnson & Johnson.

Seven years after a class action involving more than 1,350 women began, the Federal Court's Justice Anna Katzmann handed down a searing judgement in which she found Ethicon had acted negligently, and that patients should be compensated.

"We were treated like guinea pigs," one of the applicants, Julie Davis, told reporters outside court on Thursday. "They lied about it and did nothing to help."

Urogynaecological meshes, sometimes known as transvaginal meshes, are inserted into women as a treatment option for pelvic organ prolapse (when the connective tissue securing the vagina and uterus to the pelvis gives way after childbirth), or urinary incontinence.

"[Ethicon] were liable to compensate any applicant and/or group member who suffered an injury because of the defect for the amount of the loss and damage she sustained as a result of that injury," Katzmann said in an hour-long summary of her judgement on Thursday morning. "I also found that [Ethicon] engaged in misleading or deceptive conduct."

read more

[attorneygroup]

Injured by a Medical Device? Here’s What You Should Know.

Medical devices are specifically designed for medical purposes and are used to diagnose, treat or monitor a patient suffering from a particular disease or disability and improve the patient’s quality of life. Not all devices are properly tested before being marketed to consumers. In some cases, a medical device may cause serious injury or harm to a patient, and some injuries may even lead to death.

So, how do you know if a medical device is defective, or if you’ve been injured by a defective medical device? What course of action should you take if you have indeed been injured?

If you or a loved one has suffered injuries as a result of a defective medical device, contact Attorney Group for more information about your options. Affected patients and their families may be able to file a lawsuit and recover damages with the help of a defective medical device attorney.

We offer free, confidential, no obligation consultations. We can help answer your questions, and if you choose to pursue a case we can connect you with an affiliated defective medical device attorney who can assist you throughout the legal process.

The time you have to pursue a claim is limited. Contact us for more information.Get Help Now.

Common Medical Devices

Common medical devices include:

Intrauterine devices (IUD) – IUDs are small, T-shaped contraceptive devices inserted into the uterus to prevent pregnancy.

Transvaginal mesh implants – These implants are net-like devices used to treat pelvic organ prolapse and stress urinary incontinence in women.

Metal-on-metal hip replacements – Metal-on-metal hip implants are a type of hip implant in which the ball and socket components of the device are entirely made of metal.

Power morcellators – These electric surgical devices are used in laparoscopic surgical procedures (such as hysterectomy or a myomectomy) to cut up large chunks of tissue into smaller pieces.

Hernia mesh – Hernia mesh, or hernia patch, is a loosely woven sheet made from synthetic or organic material used to provide additional support to weakened or damaged tissue caused by hernias.

IVC filter – An IVC filter is a small, cone-shaped device implanted in the inferior vena cava used to catch blood clots and block their migration to the heart or lungs.

In the United States, medical devices range from simple instruments such as tongue depressors to more complex machinery such as pacemakers and programmable computer software.

Defective Medical Devices

Technological advances in medicine and the healthcare industry strive to give patients the best care possible, including the latest in medical device technology. Most products and their manufacturers want to genuinely improve the quality of life of their patients; however, some medical devices are not as safe and effective as others and can potentially cause injury or harm even when used correctly.

Patients who have suffered complications due to a defective medical device may require additional surgeries to correct any damages allegedly caused by the defective device, possibly resulting in added complications and high medical bills.

Medical device manufacturers have a legal responsibility to ensure that their products are safe for consumer use. Sometimes medical devices are put on the market without proper testing as companies are looking to boost sales and maximize profits.

Some medical devices such as knee and hip implants and permanent birth control devices are approved through the U.S. Food and Drug Administration’s (FDA) 510(k) program, a premarket device proposal which seeks to demonstrate that the device to be marketed is at least as safe and effective as an already legally marketed device. As a result, some patients may end up using a device that has been poorly tested.

What Should I Do If I’ve Been Injured by a Defective Medical Device?

If you think your medical device is defective and has caused injury, you should talk to your doctor or health care provider as soon as possible. You might also consider reporting the medical device to the FDA’s voluntary reporting program or to the manufacturer.

In some cases, your health care provider or the FDA will not be able to help you beyond treatment to alleviate your injuries and reporting of the medical device in question. If you think you might need to pursue legal action, personal injury attorneys can help you file a claim against the manufacturers of the devices for physical, emotional, and psychological pain and suffering.

The Time You Have to Pursue a Claim is Limited. Contact Us Today.

For more information, contact Attorney Group. After you contact us, an attorney will follow up to answer questions that you might have.

There is no cost or obligation to speak with us, and any information you provide will be kept confidential.

Please note that the law limits the time you have to pursue a claim or file a lawsuit for an injury. If you think you have a case, you should not delay taking action.

New Post https://attorneygroup.com/blog/defective-medical-device-information/

[designinbiology]

The most common sites of surgical mesh implantation in the pelvic floor

A | Anatomical features commonly involved in pelvic floor surgery: pelvic floor muscles and uterosacral ligament (level I support), sacrospinous ligament and arcus tendinous fascia pelvis (ATFP) (level II support) (part Aa and part Ab). The rectum is not included and the uterus is removed when necessary to obtain improve visibility. B | Transabdominal placement of polypropylene (PPL) mesh to treat pelvic organ prolapse (POP) (sacrocolpopexy operations). In these operations, the mesh is secured in a fixed position and mainly experiences a unidimensional downward force. C | Transvaginal implantation of PPL mesh at the level of the midurethra to treat stress urinary incontinence (SUI). Here, a retropubic midurethral sling is depicted. D | Transvaginal placement of PPL mesh for POP repair, 45° lateral view and 30° anterosuperior view. Many variations of these operations exist; here, how the mesh kits be can be used to fix the mesh to the sacrospinous ligament and/or the ATFP (part Da) and the tissue plane in which the mesh is implanted in mesh-augmented anterior colporrhaphy procedures are shown (part Db). In both cases, multi-axial forces are acting on the mesh and a large area of the mesh stays in close proximity to vaginal skin, making it prone to bacterial colonization. All these factors might have contributed to the occurrence of mesh-related complications.

plublished in Nature

[lgrlawfirm]

New Mesh Lawsuits Involve Hernia Mesh Complications

Many Americans have heard about transvaginal mesh implant kits (slings) that resulted in million dollar multi-district class action lawsuits for the pain and suffering caused to the women who had surgery to correct pelvic organ prolapse (POP) and stress urinary incontinence (SUI). Vaginal mesh manufacturers face tens of thousands of federal lawsuits with thousands more pending in state courts.

It now appears another medical device with troubling side effects, the C-Qur mesh, manufactured by Atrium Medical is being removed from the market. This story has not received a lot of attention and it may never get the kind of attention that the transvaginal mesh kits did. “And here is why,” explained Austin transvaginal mesh attorney Bobby Lee. “It appears the company may have initiated a ‘stealth’ recall of certain products due to allegations that C-Qur mesh increased the risks of hernia mesh complications.”

A stealth recall means a company ceases to make a certain product due to it being linked to adverse events, but does not necessarily tell the public or doctors about the move.

An Arkansas woman filed a lawsuit alleging the stealth recall. The lawsuit claims that she had a hernia repair five years ago in which the C-Qur mesh was used. Two years later, the woman began experiencing severe stomach pain and her hernia returned. This resulted in surgery to remove the C-Qur mesh. Surgeons found the mesh had crumpled inside her body and caused scarring making it impossible to replace the mesh. The woman’s hernia returned, necessitating yet another surgery — a procedure she has been unable to heal from.

According to the lawsuit she filed, Atrium Medical used an Omega 3 fish oil gel coating on the mesh, causing her body to reject it after the coating separated from the mesh. This lawsuit is not the first of its kind. There have been other patients with C-Qur implants alleging similar reactions. The suit alleges the company knew or should have known about the likelihood of mesh rejection, pain and other adverse side effects resulting from product.

More lawsuits a likely to follow  until medical device manufacturers find a way to reduce or avoid the body’s response to their products.

[alicesara611]

Pelvic Organ Prolapse Repair Device Market Report – Global Industry Analysis, Development, Scope, Share, Trends, Forecast to 2030

The global pelvic organ prolapse repair device market is projected to reach US$ 375.5 million in 2023, increasing from US$ 459.8 million in 2030, with the CAGR of 2.9% from 2023 to 2030. The increasing prevalence of POP, rising geriatric population, and growing awareness of minimally invasive surgical procedures are driving the growth of the market.

Pelvic organ prolapse (POP) is a condition in which the pelvic organs, such as the uterus, bladder, and rectum, droop or sag into the vagina. This condition can be caused by childbirth, aging, or other factors that weaken the pelvic floor muscles. POP can cause a variety of symptoms, including pain, discomfort, and urinary incontinence.

Pelvic organ prolapse repair devices are used to treat POP by supporting the pelvic organs and restoring their normal position. These devices are made of a variety of materials, such as polypropylene mesh, silicone, and titanium. They are implanted in the body through a surgical procedure.

Discover Our Expert Analysis with Our Sample Report! https://absolutemarketresearch.com/Global-Pelvic-Organ-Prolapse-Repair-Device-Market/1157/request-sample

Rising Prevalence of POP: POP is a common condition affecting women worldwide, with an estimated prevalence of 30-40% among women over the age of 50. The increasing prevalence of POP is attributed to factors such as childbirth, aging, and obesity.

Increasing Awareness of POP Management Options: There is a growing awareness among women about POP and the various management options available, including surgical and non-surgical interventions. This increasing awareness is driving the demand for POP repair devices.

Technological Advancements in POP Repair Devices: Technological advancements are leading to the development of more effective and minimally invasive POP repair devices. These devices offer advantages such as shorter recovery times, reduced risk of complications, and improved patient satisfaction.

There are two main types of POP repair devices:

Transvaginal mesh: This is the most common type of POP repair device. It is a mesh implant that is inserted into the vagina and attached to the pelvic organs and surrounding tissues. The mesh provides support to the organs and helps to prevent them from prolapsing again.

Native tissue repair: This type of POP repair device does not use mesh. Instead, the surgeon uses sutures to repair and tighten the weakened muscles and tissues that support the pelvic organs.

The type of POP repair device that is right for you will depend on your individual circumstances and the severity of your prolapse. In some cases, a combination of a transvaginal mesh and native tissue repair may be used.

Benefits of POP Repair Devices:

Relieve symptoms of POP: POP can cause a variety of symptoms, such as urinary incontinence, bowel incontinence, and pain during intercourse. POP repair devices can help to relieve these symptoms.

Improve quality of life: POP can have a significant impact on a woman's quality of life. POP repair devices can help women to regain their independence and participate in activities that they may have had to avoid due to their prolapse.

Prevent further prolapse: POP can recur without treatment. POP repair devices can help to prevent further prolapse from occurring.

Regional Analysis:

North America is expected to hold the largest share of the global POP repair device market throughout the forecast period. This dominance is due to factors such as high prevalence of POP in North America, well-established healthcare infrastructure, and early adoption of new technologies.

Europe is expected to be the second-largest market for POP repair devices. The European market is driven by factors such as increasing awareness about POP, aging population, and growing demand for minimally invasive procedures.

The Asia Pacific market is expected to experience the fastest growth during the forecast period. This rapid growth is attributed to factors such as rising prevalence of POP in the region, increasing disposable incomes, and growing urbanization.

Key Players:

The global POP repair device market is characterized by the presence of a number of global and regional players. Some of the key players in the market include:

Boston Scientific Corporation

Johnson & Johnson/Ethicon

Medtronic plc

AMS/Uromed

Coloplast A/S

B. Braun Melsungen AG

Spacelabs Healthcare, Inc.

Bard Medical, Inc.

Cook Medical

Tensoplast

Segmentation:

The global POP repair device market can be segmented based on the following factors:

Product Type:

Transvaginal Tapes

Burch Colpocleisis

Sacrocolpopexy

Others

End-User:

Hospitals

Ambulatory Surgical Centers

Clinics

Geography:

North America

Europe

Asia Pacific

Latin America

Middle East and Africa

[lawyer4help]

HOW TO KNOW IF YOU ARE SUFFERING FROM VAGINAL MESH COMPLICATIONS

Lawyer4Help helps women file Bladder sling lawsuit in USA who have gone through vaginal mesh complications. We provide the best lawyers who have experience in legal proceedings on these cases and reaching a fair settlement.

Pelvic organ prolapse occurs when childbirth and such conditions wear out the tissue in the pelvic area which leads to pain and discomfort. Doctor recommends mesh surgery in the time of an emergency.

Tansvaginal mesh, also known as pelvic mesh or bladder sling. It is a surgical material made of non-absorbable/absorbable synthetic polypropylene that is used to give an extra support to pelvic organ. It is implanted during a surgical procedure for mending a weakened and damaged pelvic organ.

Although, the mesh surgery causes severe complications on account of the problems linked with the procedure. According to FDA, surgical mesh complications are frequent to encounter and ultimately reclassified the use of mesh from moderate to severe risk.

Complications you may face

Frequent complications reported so far from transvaginal surgery include:

● Vaginal mesh erosion

● Infection

● Pelvic and near organ perforation

● Vaginal Shrinkage

● Urinary problems

● Neuro-muscular problem

● Trouble walking

● Fever on and off

● Nausea

● Weight loss

Some of the news reported in the past where women faced urinary issues where every time they laugh, cough, sneeze or part in activities that create extra pressure, causing a small amount of urine to leak. In some cases, it was frequently identified that women wore sanitary pads in defense.

Based on Doctor Raz's experience, 20 to 30% of complications he named as “lupus type”, results in runny nose, muscle pain, fogginess and lethargy.

Primary reason behind facing difficulty is when the mesh starts eroding in the vagina. This makes the mesh slip off of the implanted position and lead to harming pelvic organs and its surroundings.

Symptoms of mesh complications

Vaginal mesh complication symptoms occur within week or month of the surgery which include:

● Painful intercourse

● Vaginal bleeding

● Intensifying urinary incontinence

● Vaginal discharge and pain

These symptoms worsen over time. It’s required to become aware of the symptoms and take prompt actions before it’s late. Besides medical treatment, it’s needed to spread awareness and get justice from it. Bladder Sling lawsuits helped many women and brought them to justice by huge settlements.

Recommendations for women who face complications

Consult a specialist in this area with significant surgical skills and start medical treatment at the earliest.

Other than this as you’ve learned how claiming an amount from companies is beneficial. It not just fulfills your financial loss but stimulates your mental state with a sense of fairness and aids to share knowledge vastly.

Let’s get into a few facts.

Women who have sued companies over vaginal mesh have pulled off success of at least around $300 million. By 2017, many companies had settled thousands of demands for millions of people.

There was a case of Sherise Grant among many women who had faced urinary problems, she pulled off a settlement of $8 billion.

One patient has achieved a victory of $41 million verdict against Johnson & Johnson. Other times the jury awarded millions of dollars to patients. In the meantime, 108,008 lawsuits have been filed in the MDLs and reaching settlements.

In August 2021, FDA banned Boston Scientific and Coloplast devices for transvaginal repair of pelvic organ prolapse to be available for commercial use.

Based on all the factuality, we recommend you to get in touch with the right attorneys on time. Lawyer4Help has experience in giving individuals the power to work out their legal rights in many matters and provides Best lawyers to you.

Settle your Transvaginal mesh lawsuit claims with us. We make things right for you!

[garciaphan]

Taking Legal Action Against Manufacturers And Distributors Of Problematic Products

Medical devices that don't work properly can make an already bad situation worse. In order to maintain the best possible quality of life, patients rely on these tools. When it comes to keeping a loved one alive, a device or instrument's performance can make all the difference.

 Despite the fact that every medical procedure carries some level of risk, some complications can be traced directly back to a manufacturer's oversight. Products liability cases involving flaws in product design, inadequate notice of product features, or flaws resulting from inconsistent construction can be complicated legally by the attorneys At Garcia & Phan, we have over 40 years of combined legal experience and can help fight for your personal injury claim. We offer free case reviews and will not charge any legal fees unless we obtain compensation for you.

 Products Frequently Found To Be Defective

 Some products are more closely linked to serious outcomes than others, but any tool or device can be defective. Regardless of how simple or complex a product is to make, it is the responsibility of the manufacturer to create safe and dependable devices.

 Lawsuits alleging product liability often centre on mesh implants. Complications from transvaginal mesh surgery, for example, have the potential to seriously harm a patient's organs. If the surgical mesh used to treat hernias is flawed, it could puncture organ tissue or result in a second hernia.

 There are other types of implants that can fail, even if they are meant to support vital bodily functions. There have been instances where blood flow management and heart protection devices, such as IVC filtration, have failed in our firm's experience. There may be no life-threatening consequences from faulty implants, but they can still have a major impact on the patient's quality of life.

   Fighting Financial Consequences Of A Product

 Our lawyers can estimate the potential value of a successful lawsuit if an individual, group, or company has suffered a significant financial loss as a result of a product. Many of our clients were able to move forward after being injured as a result of a defective product. As well as compensation for unjustified expenses, we are adept at arguing for the return of lost interest or wage.

 Contact Garcia & Phan Law Firm through the online intake form or by phone at 714-586-8298 for a thorough case review.

[perhaps-we-fly]

”We should be concerned if our health system is forced to prioritise convenience and financial targets over wellbeing of its patients. The vaginal mesh is causing chronic burning pain, organ erosion, bladder and bowel perforation, tissue damage, and some women are even left wheelchair-bound or dead. These women’s lives and sex lives are being ruined - but not just theirs. Some report that the mesh has sliced through the vaginal walls, cutting the man’s penis during sex. That ought to finally get everyone’s attention.”

[bluepointcoin]

Canadian women with transvaginal mesh implants to share $21.5 million in settlement A group of Canadian women who suffered ill-effects from implantation of a medical device called transvaginal mesh will receive a total of $21.5 million in compensation, recent court records show. Source link