Posts Tagged ‘Colorado Springs’
Hip Replacement LawsuitsMany of the Hip replacement manufacturers of the metal-on-metal hip implants have recalled their implants for functional defects. There have been settlement offers on hip replacements for victims of a faulty hip implant or cobalt and chromium poisoning to the blood stream.
Hip Replacement Revision Surgery LawsuitsHip replacement or revision surgery is one of the most common orthopedic procedures performed in the United States. There have been numerous defective implants placed on the market resulting in needles pain, suffering and revision surgeries
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Below is a list of cases our hip replacement lawyers will take a look at.
- Stryker Rejuvenate Modular Neck Cases – All
- Stryker ABG II Modular neck Cases – All
- Stryker Accolade (TMZF) Stem cases with Cobalt Chromium modular heads. These stems have the potential for significant head neck corrosion – All cases with Metallosis.
- Wright Medical Conserve Cup (MOM) cases – ALL
- Wright Medical Profemur Stem Cases (this is their modular neck design)- These cases are prone to Fracture (either the titanium or CoCr necks) and Metallosis. ALL.
- Depuy ASR – ALL
- Depuy Pinnacle Metal on Metal (MOM) with modular heads greater than 36 mm.
- Zimmer Durom Cup cases with modular heads greater than 36 mm.
- Zimmer M/L Taper Kinectiv Stem cases (this is their Modular neck design)- All cases with Metallosis.
- Biomet M2A 38mm / Magnum MOM cases. ALL cases with Metallosis.
- DJO / Encore MOM hip cases. All cases revised due to Metallosis.
- Omnilife Apex Arc – This is a smaller manufacturer but this device is a mixed metal modular neck device. ALL
- Smith & Nephew R3 (MOM) cup cases. Only cases that have metallosis and were revised or need a revision.
- Smith & Nephew SMF stem (this is their mixed metal modular neck product). We have not seen many of these yet but, our hip replacement lawyers are interested in them.
- Zimmer’s NexGen Natural Knee System implant lawyers,
- Stryker’s Scorpio implant lawyers,
- Smith & Nephew’s OXINIUM devices lawyer.
Knee Replacement ComplicationsComplications Lawsuits are Being Filed For: Persistent pain, swelling or stiffness, Deep vein thrombosis, Implant failure within five years, Nerve injuries, Fracturing, chipping and migration and Infections.
Brand Knee Replacements Lawsuit FilingsKnee Replacements Causing Problems Include: DePuy knee, Zimmer NexGen LPS, CR and MIS, Natural Knee System, Stryker Scorpio CR and PS components, Duracon Total Knee, Unicompartmental Knee System, Smith & Nephew Oxinium Genesis II and Profix II, Journey Uni Tibial Baseplate, and Biomet Vanguard CR.
Knee Replacement RecallsHas your knee replacement caused debilitating side effects? Have you needed to undergo revision surgery to fix or replace the device or to correct complications caused by the device?
Complications resulting in a knee replacement recall include:Persistent pain of recipient, Infection or drainage, Swelling or inflammation, Damage to surrounding bone, muscle, or nerves
Zimmer NexGen Knee RecallsWhile there has not been a total recall on any Zimmer NexGen knee replacement devices, a number of device components have been recalled. In 2010, Zimmer NexGen MIS Tibial Components were recalled due to high incidences of failure associated with the components. The Zimmer NexGen LPS-Flex GSF Femoral Component was also recalled due to evidence of loosening. Additionally, the Zimmer Natural-Knee II Durasul Patella faces a Class II recall. This component is not part of the Zimmer NexGen product line.
Zimmer RecallsZimmer NexGen knee recalled components include: NexGen MIS Tibial Components,NexGen TM Tibial Trays, NexGen LPS-Flex GSF Femoral Component, NexGen MIS Modular Tibial Plates and Keels.
Stryker Knee Replacement RecallsIn April 2013, the FDA issued a Class I recall of Stryker’s ShapeMatch Cutting Guide. The Guides help to position knee replacement components and guide the marking of the patient’s bone prior to cutting. In November 2012, Stryker acknowledged manufacturing defects in the ShapeMatch Cutting Guide and instructed surgeons to discontinue use. This knee replacement recall was because the software has a defect that causes wider cutting ranges. As a result, knee replacement patients may experience severe complications such as instability of the joint, fracture, chronic pain, and mobility limitations. Patients may also require the need for revision surgery.
Other Knee Replacement RecallsStrykerDuracon Total Knee, Unicompartmental Knee System, Scorpio PS and CR components, BiometVanguard CR, Smith & Nephew Journey Uni Tibial Baseplate, Oxinium Genesis II and Profix II
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Bard IVC Filter DangersBard IVC Filters have certain dangers. The filters can fracture and pieces can migrate and perforate various organs in the body. Inferior Vena Cava filters are implanted to capture blood clots before they can settle in the brain or lungs resulting in a pulmonary embolism or stroke.
Bard IVC Filter Lawyers Filing Inferior Vena Cava Lawsuits For a Failed
- Bard Recovery filter;
- Bard G2 filter;
- Bard G2 Express filter;
- Cook Gunther Tulip
Vena Cava Filter Lawsuits Filed
What are the Complications Of The Bard IVC Filters?Fracture of the Cook IVC Filter, Bard IVC Filter Migration, Perforation, Puncture or Serious Damage to the Heart, Lungs or Vena Cava, Internal Bleeding, Hematoma or Nerve Injury at the Puncture Site of the Bard IVC Filter, Inferior Vena Cava Filter related Pulmonary Embolism, Respiratory Distress From the IVC Filter, Infection from the IVC Filter, Shortness of Breath, Death
Get a Bard Inferior Vena Cava Filter Lawyer File Your Bard IVC Filter Lawsuit
Do You Want To File A Talcum Powder Lawsuit?If you have used talcum powder or baby powder products and developed ovarian cancer you may be able to file a Talcum Powder lawsuit Current lawsuits Johnson & Johnson claim that long-term use of talc-based products caused women to develop ovarian cancer. Victims claim that they were not warned of the risks associated with these talc products. Women and their families may be able to seek compensation for ovarian cancer diagnosis with the help of one of our lawyers.
Is There A Risk of Talcum Powder Causing Ovarian Cancer?Talcum powder lawsuits claim Talcum Powder caused ovarian cancer. When used as a feminine hygiene product, talc particles can travel through the vagina and into the ovaries and remain trapped for years. These talc particles can cause inflammation and eventually lead to the growth of ovarian cancer cells.
Studies Claim Dangers Of Talcum PowderAlthough Johnson & Johnson maintains that talcum powder is safe for use, plaintiffs in ovarian cancer lawsuits offer studies that suggest an association between talc and ovarian cancer dating as far back as 1971. In 1994, Johnson & Johnson was put on notice of a link between talc and ovarian cancer. A letter was sent from the Cancer Prevention Coalition to the then-CEO of the company.
Will There Be a Talcum Powder Ovarian Cancer Class Action Lawsuit I Can Join ?According to news reports, more than 1,200 women claim talcum powder caused their ovarian cancer. Currently the lawsuits are being filed at the state level.
Talcum Powder Lawsuit SettlementsA $72 million talcum powder verdict is handed down against Johnson & Johnson in favor of a woman who claimed that long-term Shower-to-Shower use for feminine hygiene caused her to develop ovarian cancer. The verdict included a $62 million award of punitive damages against the company. Our talcum powder cancer lawyers are available to discuss your options.
It has become apparent that there is a large number of drugs and devices class actions that have been filed against manyfacturers that have targeted women.
We can start with the Dow Corning siicone breast implant class action of years ago. Women are still suffering today. The Dow Corning Trust just recently launched a silicone breast implant explant program. The leaking silicone and bursting implants lead to toxicity related immune system diseases like lupus and fibromylagia and other immune deficiency diseases. Women to this date are still suffering from their Dow silicone Breast Implants and the Dow Corning settlement trust is stll living out payments like the new breast explant program.
Fosamax was supposed to cure osteoporosis but ended up causing femur fractures.Then we have Yaz and Yasmine birth control pills. Young women were having their lives altered by pre-mature strokes, pulmonary embolisms, deep vein thrombosis, blood clots and heart attacks. Many girls harmed were barely starting a college life.
History moves along to the metal on metal and metal componednt hip replacements like the DePuy Pinnacle and ASR Hip Replacement and the Stryker Rejuvinate and ABG II Modular Stems. These are a metal on metal hip replacement recalled for their need for revision surgery. These hip replacements failed in women more then men. The smaller frame of a women makes the device more prone to problems in the female structure.
NuvRing has been another disaster for women causing:
blood clots in women
cerebral thrombosis in women
deep vein thrombosis
heart attack in women
retinal thrombosis in women
stroke or cerebral hemorrhage
thrombophlebitis and venous thrombosis with or without embolism
toxic shock syndrome
Fosamax for osteoporosis actually causes what it is prescribed to fix , femur fractures.
Vaginal Mesh Lawsuits
The biggest and most horrific is the the various vaginal mesh devices for urinary incontinence and uterine, bladder and bowel prolapse. This mesh device is made of a Prolene plastic synthetic fiber that has been falling aprt in women. Thousands of women across the country are screaming the horrors of the vaginal mesh and lawsuits are being filed in droves. Women are in severe pain described as razor blades. The mesh has been reported by female victims to be eroding thru the vaginal wall and at times into the bladder and bowel. Women can no longer have sexual intercourse and marriages are falling apart. Women are losing their jobs and cannot work. And then we have the Mirena IUD which has been gravitating our of postion and ending up embedded in the uterus or a nearby organ.
Lives are being ruined and justice must be sought. Lawsuits are the only thing these manufacturers understand.
We continue to accept nationwide vaginal mesh and bladder sling cases, Actos lawsuits, NuvaRing lawsuits, Dialysis medication lawsuits, Pradaxa lawsuits, Hip Replacement lawsuits, SSRI birth defect lawsuits, Tylenol lawsuits, Yaz lawsuits and others.
Nationwide vaginal mesh and bladder sling cases
Patients have been diagnosed with bladder cancer after consuming the diabetes drug Actos.
Chemical Toxins Leach V Dupont Class Action Lawyers
Patients diagnosed with kidney cancer, testicular cancer, ulcerative colitis and/or thyroid disease who are members of the Leach v. Dupont class. Leach class definition: a person who drank contaminated water for at least one year prior to December 3, 2004 from one of six named water districts, or specified private drinking water wells contaminated with C-8. The affected water districts are:
Patients diagnosed with kidney cancer, testicular cancer, ulcerative colitis and/or thyroid disease who are members of the Leach v. Dupont class. Leach class definition: a person who drank contaminated water for at least one year prior to December 3, 2004 from one of six named water districts, or specified private drinking water wells contaminated with C-8. The affected water districts are (1) Little Hocking, Ohion (2) Lubeck Public Service District, West Virginia (3) City of Belpre, Ohio (4) Tuppers Plains, Ohio (5) Mason County Public Service District, West Virginia (6) Village of Pomeroy, Ohio.
Chemical exposure lawyer Little Hocking,
Chemical exposure lawyer Lubeck Public Service District,
Chemical exposure lawyer Belpre,
Chemical exposure lawyer Tuppers Plains,
Chemical exposure lawyer Mason County Public Service District,
Chemical exposure lawyer West Virginia ,
Chemical exposure lawyer Village of Pomeroy
It does not matter where class member now reside, so long as they lived in one of the contaminated areas and drank the water at least one year effective December 3, 2004.
DePuy Hip Pinnacle and ASR Hip Implant Recall Lawyers
Faulty Metal-on-Metal Hip Implants.
We are actively pursuing new Fosamax femur fracture cases. Our intake criteria for these cases is as follows: (1) proof of at least 4 years of Fosamax use or other oral bisphosphonates; (2) fracture of the subtrochanteric or shaft area of the femur; (3) no or minimal trauma associated with the fracture; (4) 80 years old or younger at time of fracture.
Granuflo, Naturalyte Dialysis Mediction Lawyers
We are litigating cases aagainst Fresenius, the German manufacturer and distributor of GranuFlo and NaturaLyte dialysate products. These products are supposed to safely filter and cleanse the bloodGranuFlo/NaturaLyte has been directly linked to unsafe levels of bicarbonate in dialysis patients.
Accepting cases preferably for injuries arising after 2011. Organon/Merck’s vaginal ring contraceptive drug/device are being actively litigated in both state and federal venues, and have been since late 2007. Plaintiffs allege that NuvaRing increases a woman’s risk of blood clots, heart attack, and stroke above and beyond the risk that is mentioned in the label.
Pradaxa Excessive Bleeding Lawyers
Pradaxa is an anticoagulant drug indicated for patients who have been diagnosed with atrial fibrillation. Pradaxa was heralded as a treatment advance because it is easier to take than its competitor, it also can cause uncontrollable bleeding which cannot be stopped by any antidote. Accordingly, there have been bleeding events which have lasted for days. Some clients have been told that there is simply nothing medical science can do to stop the bleeding. People have died
Lexapro/Celexa, Zoloft, Prozac, Effexor, Wellbutrin and Pax Lawyers
SSRI antidepressant manufacturers, including Glaxo-SmithKline, Eli Lilly, Pfizer, and Forest Laboratories, alleging a variety of birth defects from prenatal exposure to these drugs. The products involved include Lexapro/Celexa, Zoloft, Prozac, Effexor, Wellbutrin and Paxil.
Stryker Hip Replacement Lawyers
Litigation against Stryker. “Rejuvenate” and “ABGII” stem implants were recalled in the summer of 2012, and the failure of these femoral stems has caused enormous damage for those patients as a result of “fretting” in the modular neck- stem junction, leading to corrosion and exposure to large amounts of metallic debris.
Tylenol Lawyers For Liver Damage
Branded Tylenol acetaminophen toxicity causing acute liver failure requiring hospitalization.
*Only for injuries that occurred before 4/10/2012 as well as from states with 3+ year SOLs and Discovery rules. Cardiovascular injuries caused by Drospirenone (DRSP), the active progestin component in these oral contraceptive pills. Deep Vein Thrombosis, Pulmonary Embolism, Blood Clots and certain types of Stroke.
Bladder Sling Lawyers, Bladder Sling Lawyers Filing Nationwide Bladder Sling Lawsuits
The bladder sling lawyers of Class Action Lawyer Network are accepting all nationwide bladder sling lawsuits. Lawsuits are being filed as a part of the consolidated MDL'S in West Virginia.
What Is A Bladder Sling?
Bladder slings are used to treat urinary incontinence by implanting a sling around the urethra. The bladder sling is attached to the abdominal wall or pelvic bone. The bladder sling is a vaginal mesh device, and has all the complications for which TVT lawsuits are being filed.
Bladder Sling Complications
Erosion thru the vaginal wall
Erosion into the bladder,
Pain during sexual intercourse,
Perforation of bladder, colon,
Our bladder sling lawyers are filing bladder sling lawsuits for women. You must file a bladder sling lawsuit quickly, as the statute of limitations is running very close in many states.
The manufacturers are:
Bard Avaulta Support System MDL No. 2187
AMS Elevate Prolapse Repair System MDL No. 2325
AMS Apogee Vault Suspension System
AMS Perigee System
AMS Monarc Sling System
AMS Sparc Sling System
Ethicon Gynecare Gynemesh MDL No. 2327
Ethicon Gynecare Prolene Soft Mesh
Ethicon Gynecare Prolift Pelvic Floor Repair System
Ethicon Gynecare TVT Transvaginal Sling
Boston Scientific Pinnacle Pelvic Floor Repair Kit MDL No.2326
Boston Scientific Uphold Vaginal Support System
Vaginal Mesh Multi District Lawsuit List Consolidated Under Judge Goodwin in West Virginia
MDL – 2325, IN RE: American Medical Systems, Inc., Pelvic Repair System Products Liability Litigation
MDL No. 2187 | In RE: CR Bard, Inc., Pelvic Repair System Products Liability Litigation
MDL – 2326 IN RE: Boston Scientific Corp. Pelvic Repair System Products Liability Litigation
MDL – 2327 IN RE: Ethicon, Inc., Pelvic Repair System Products Liability Litigation
Our experienced bladder sling lawyes ready to file bladder sling lawsuits slings problem lawsuits. Vaginal mesh products have many different names. Do not assume your bladder sling is not covered in the TVT lawsuits until you speak to one of our bladder sling lawyers. Many states have a statue of limitations issue. Time is of the essence. Call our nationwide bladder sling lawyers today.
Lipitor lawyers of Class Action Lawyer Network are filing lawsuits for women who are getting type 2 diabetis from lipitor.
Lipitor is prescribed to lower her cholesterol levels and help decrease the risk of developing cardiovascular disease. However, after using the medication many women are being d diagnosed with type 2 diabetes.
It appears Pfizer knew about the increased risk of diabetes from Lipitor, but failed to provide adequate warnings for women and their doctors.
Lipitor Is Causing Type 2 diabetes in women taking Lipitor
What Is Lipitor?
Lipitor (atorvastatin) is one of the most widely used brand-name medications in the United States. Millions of people take the medication to help lower cholesterol. Pfizer had more than $125 billion in Lipitor sales.
FDA Warning For Lipitor
In February 2012, the FDA required new diabetes warnings for Lipitor. This was due to the increased risk of changes to blood glucose levels.
Lipitor lawyers are filing Lipitor lawsuits
Mullti District Litigation Consolidation For Lipitor Lawsuits
U.S. Judicial Panel on Multidistrict Litigation (JPML) rejected a request filed by Lipitor lawyers to centralize all cases brought in the federal court system. The MDL panel has determined that each of the cases will proceed as individual lawsuits in the U.S. District Court where they were filed.More than half of the pending actions are already consolidated before one judge in the District of South Carolina.
If you or a loved one has been diagnosed with Type II Diabetis after taking Lipitor contact us to speak toa Lipitor lawyer today.
Yaz, Yasmin Lawsuit Multidistrict Litigation
MDL 2100 – Yasmin and YAZ (Drospirenone) Marketing, Sales Practices and Products Liability Litigation, multidistrict litigation (MDL) in Illinois federal court.
Yaz lawyers are accepting Yaz lawsuits for blood clot related injuries:
- Pulmonary Embolism
- Blood Clots
- Deep Vein Thrombosis
Bayer is facing thousands of Yaz and Yasmin lawsuits involving blood clot related injuries.
Yaz Blood Clot Settlements
According to Bayer’s 2nd Quarter 2013 Statement, Bayer haa agreed to pay more than $1.4 billion to resolve an estimated 6,700 lawsuits from women who suffered a:
Heart attack or Stroke from Yaz or Yasmin
Pulmonary Embolism from Yaz or Yasmin
Deep Vein Thrombosis from Yaz or Yasmin
There are still more than 5,000 additional claims involving a thrombosis blood clot related injury. Bayer is continuing negotiating on a case-by-case basis, after complete documentation and presentation of the claim by an attorney. It is not too late to file your Yaz blood clot lawsuit. Our Yaz lawyers are still continuing to review and evaluate potential claims from women who suffered a pulmonary embolism, deep vein thrombosis, heart attack, stroke or other blood clot injury while using Yaz, Yasmin or Ocella.
If you or a loved one has been injured by Yaz or a loved one has died from a Yaz related injury call us for a Yaz lawyer today.