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.
Have You Been Contacted By A Representative Company Offering To Pay For Your Hip Implant Revision Surgery?
Speak to a Stryker lawyer first. The offer is very specific and uses two very important words. They are "if necessary". We do not know what the definition and criteria of "if necessary" is.
Stryker Hip Implant Lawsuits Have Been Consolidated In A Massive Litigation
Lawsuits filed in U.S. District Courts against hip implant maker Stryker Corporation over the recalled Rejuvenate and ABG II hip components have been consolidated in Minnesota in a multidistrict litigation, or MDL. This order took effect June 12, 2013 when the federal Judicial Panel on Multidistrct Litigation ordered 41 Stryker hip lawsuits from 16 different federal districts to be consolidated under the the Honorable Judge Donovan W. Frank.(In Re: Stryker Rejuvenate and ABG II Hip Implant Products Liability Litigation, MDL No. 2441) for
Stryker hip implants.
Many More Lawsuits Are Anticipated
This consolidation may also encourage Stryker lawsuit settlements. All recipients of a Stryker ABG II Modular Stems or Rejuvinate hip implant needing revision surgery are advised to file their Stryker Hip Replacement Lawsuit.
Have you received a recall letter from Stryker?
Have you been told you need revision surgery?
Have you already gotten revision surgery?
Speak to one of our Stryker Hip Replacement lawyers today before accepting any offers or signing anuy paperwork.
The following dangrous drugs and devices are appearing in lawyer ads and email blasts across the country.: Vaginal Mesh, Transvaginal Mesh, Pelvic mesh, Surgical mesh, Bladder sling, Stryker Rejuvinate hip replacement, Stryker ABG Modular II Stems, Yaz, and Mesothelioma. The following dangrous drugs and devices are appearing in lawyer ads and email blasts across the country.:
Vaginal Mesh Lawsuits
Women nationwide in the thousands are filing vaginal mesh lawsuits for severe mesh complications. The vaginal mesh lawsuits have been consolidated and the bellwether trials are moving ahead.
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 – 2326 IN RE: Boston Scientific Corp. Pelvic Repair System Products Liability Litigation
MDL – 2327 IN RE: Ethicon, Inc., Pelvic Repair System Products Liability Litigation
MDL – 2387 IN RE: Coloplast Corp. Pelvic Support Systems Products Liability Litigation
TransVaginal Mesh Lawsuits
These are still the same Prolene mesh which is causing severe complication, just unsder another name
Pelvic Mesh Lawsuits
Still the same Prolene mesh and vaginal mesh lawyers, transvaginal mesh lawyers, and pelvic mesh lawyers are filing vaginal mesh lawsuits for all of these
Surgical Mesh Lawsuit, Bladder Sling Lawsuits
Still the same vaginal mesh lawsuit products
Stryker Rejuvinate and ABG Modular II Stems Hip Replacement
Class action Stryker lawsuit lawyers are filing lawsuit for the failed Stryker hip replacement where revision surgery is needed. We suggest you see an orthpedic doctor immediately.
The U.S. Judicial Panel on Multidistrict Litigation is considering forming an MDL to handle the growing number of Stryker lawsuits. Both the Rejuvenate and the ABG II hip implants were recalled in July 2012. This was done due to reports that the implants were causing complications including loosening of the joint, corrosion, and increased risk of inflammation as well as metal toxicity. Many victims of these failed devices have had to undergo revision surgery to remove and replace them long before they reached the end of their expected 15-20 year lifespan. On March 18, 2013, Stryker filed a brief with the JPML, agreeing that coordination of lawsuits involving the recalled devices was appropriate.
Yaz class action lawyers are accepting Yaz cases for blood clots, stroke, pulmonary embolism and untimely death of young women.
As of February 12, 2013, Bayer had reached agreements, without admission of liability, to settle the claims of approximately 4,800 Yaz victims in the U.S. for a total amount of about US$1 billion," according to the annual report.
Bayer also said that it, "is only settling claims in the U.S. for venous clot injuries (deep vein thrombosis or pulmonary embolism) after a case-specific analysis of medical records on a rolling basis. Such injuries are alleged by about 3,200 of the pending unsettled claimants. Bayer will continue to consider the option of settling individual lawsuits in the U.S. on a case-by-case basis.
1000's of hard working citizens are starting to show signs of mesothelioma from asbestos exposure on the job. Class action lawyers for Mesothwlioma victims and their families are here to help you.
Stryker has recalled a number of hip replacements including: Stryker Rejuvinate, Stryker ABG II and the Trident. Lawsuits are being filed against Stryker for implant failure of all these devices
Stryker recalled its Trident artificial hip in 2007 due to device failures in recipients. Previous plaintiffs have cited symptoms consistent with other defective metal-on-metal hip implants, along with one defect that was unique to the Trident device: Many recipients claimed of hearing a loud squeaking noise coming from their hip region after receiving this particular model.
Stryker recalls on the Rejuvinate and ABG II will effect thousands and the lawsuits are coming in in mass. The FDA has taken another look and is proposing changes to regulations that allowed two Stryker Corp. recalled hip implant systems to be deemed safe. But the move does little for the tens of thousands of patients already implanted with the faulty medical devices. The DePuy Pinnacle and ASR are other failed recalled hip replacements that have injured thousands of victims. The FDA proposed changes for the 510(k) Premarket Notification Process for the approval of metal-on-metal hip implants like those manufactured by Stryker and DePuy come very late for seniors burdened with painful revision surgeries.
In July 2012, after injured patients filed more than 60 adverse event reports with the FDA, Stryker issued a voluntary recall of its ABG II and Rejuvenate hip implant systems. Post-market surveillance revealed that a metal-on-metal junction in these devices can shed metal debris, causing pain and tissue damage that may require a revision surgery. Can the FDA actually step up to the plate and protect our citizens?
The FDA’s most recent proposal aims to standardize the requirements for how the agency accepts data, regardless of the submission or application type. The new regulation will require 510(k) submissions to be scrutinized by an institutional review board (IRB), a must for PMA applications.
The proposal for better practices in approval of medical devices like hip implants would become effective 180 days after publication, and the proposal to shift from 510(k) to PMA for metal hips would become effective 90 days after publication. Lawyers for Stryker and Depuy hip replacements are filing lawsuits for failed devices.