Seithel Law, LLC

Seithel Law, LLC Seithel Law, LLC represents people who suffer catastrophic injuries. Seithel Law, LLC's clients have injuries they relate to dangerous pharmaceuticals.

FDA RECALLAvKARE Sildenafil 100mg tablets National Drug Code: 42291-748-01Trazadone 100mg tablets National Drug Code: 42...
12/10/2020

FDA RECALL
AvKARE
Sildenafil 100mg tablets National Drug Code: 42291-748-01
Trazadone 100mg tablets National Drug Code: 42291-834-10

According to the company, the Sildenafil lot may contain Trazadone and the Trazadone lot may contain Sildenafil.

Sildenafil is for erectile dysfunction and Trazadone is for treatment of major depressive disorder.

If you have any of these lot numbers and have suffered an adverse reaction, feel free to contact us. Please do not dispose of the medication or their containers.

2018 WORST CORPORATE CONDUCT......
12/11/2018
American Association for Justice

2018 WORST CORPORATE CONDUCT......

AAJ’s new research report, Worst Corporate Conduct of 2018, examines many examples of corporate abuses at the expense of citizens, consumers, employees, and investors. Read our report to learn more about the role of civil justice in the fight against corporate misconduct.

Redbarn Pet Products Issues Voluntary Recall of Dog Chews
02/12/2018
Redbarn Pet Products Issues Voluntary Recall of Dog Chews

Redbarn Pet Products Issues Voluntary Recall of Dog Chews

With an extreme abundance of caution, and with the care and concern of pets top of mind, Redbarn Pet Products, LLC of Long Beach, CA is voluntarily recalling a single product, Redbarn’s 7-inch Bully Stick three pack, because it has the potential to be contaminated with Salmonella. Salmonella can a...

05/16/2017
www.fda.gov

FDA links increased risk of leg and foot amputations to Invokana, Invokamet, and Invokamet XR.

Contact Seithel Law, LLC if you or a loved one has suffered leg or foot amputation after taking Invokana, Invokamet or Invokamet XR.

Study Shows Medical Errors 3rd Leading Cause of Death....
05/04/2016
Medical Errors Are No. 3 Cause Of U.S Deaths, Researchers Say

Study Shows Medical Errors 3rd Leading Cause of Death....

If not for flawed classification of deaths, medical mistakes would be the third leading cause of U.S. deaths, Johns Hopkins researchers say. They're calling on the CDC to track deaths from errors.

Following the $76 Million dollar verdict in February....Please contact us if you or your loved one used talcum powder pr...
05/03/2016
BREAKING: J&J Hit With $55M Verdict In Ovarian Cancer Trial - Law360

Following the $76 Million dollar verdict in February....Please contact us if you or your loved one used talcum powder products and developed ovarian cancer. 800-818-5329

A Missouri state jury on Monday awarded $55 million to a woman suing Johnson & Johnson alleging she developed ovarian cancer after decades of using talc baby powder on her genitals, marking a second major defeat for the company in as many trials over the alleged talc-ovarian cancer link.

FDA takes additional action to better understand safety of Essure, inform patients of potential...
03/22/2016
FDA takes additional action to better understand safety of Essure, inform patients of potential...

FDA takes additional action to better understand safety of Essure, inform patients of potential...

The U.S. Food and Drug Administration announced today two actions to provide important information about the risks of using Essure and to help women and their doctors be better informed of the potential complications associated with implantable forms of sterilization. These actions include a new, ma…

Seithel Law, LLC is currently evaluating claims for women who have experienced adverse events with the Essure Permanent ...
11/25/2015
Essure Permanent Birth Control

Seithel Law, LLC is currently evaluating claims for women who have experienced adverse events with the Essure Permanent Birth Control.

Essure Permanent Birth Control Share Tweet Linkedin Pin it More sharing options Linkedin Pin it Email Print Update on the status of FDA’s evaluation of the Essure SystemEssure is a permanent birth control method for women (female sterilization). Implantation of the Essure System does not require a s…

They tested the pill on men....only 10% efficacy.....cancers in the mice studies ...good for women????
09/22/2015
Female Libido Pill Caused Dissent in FDA Ranks, Memo Shows

They tested the pill on men....only 10% efficacy.....cancers in the mice studies ...good for women????

Addyi, the pink pill for women with low libido, was approved by the Food and Drug Administration last month even though at least three FDA reviewers recommended rejecting it.

09/11/2014

Boston Scientific was Ordered to Pay $73 Million by a Dallas Texas jury for liability for Martha Salazar's injuries which she blamed on Boston Scientific's Obtryx sling. The jury awarded her approximately $23 million in compensatory damages and $50 million in punitive damages.

In 2012 the FDA ordered Boston Scientific, Johnson & Johnson and more than 30 other vaginal-implant makers to study rates of organ damage and complications linked to their products. Juries in New Jersey and West Virginia over the past year have ruled that Johnson & Johnson and Bard implants caused women's TVM injuries and ordered the companies to pay more than $13 million.

In the Salazar case, the Dallas jury returned the verdict the same day it began deliberations. They found that the Obtryx sling suffered from a faulty design and that the company failed to properly warn patients and doctors about the health risks associated with the sling. Reports are that as part of the evidence in the case, lawyers for Salazar presented an August 2000 email from a Boston Scientific executive which told sales people to ignore a company funded study raising questions about the sling's safety and quoted, "I certainly wouldn't hand this out to any physicians," the Boston Scientific executive said in an email.

If you or your loved ones were injured by trans-vaginal mesh, please call on us today for a free consultation. Seithel Law, LLC represents women who underwent revision surgery as a result of complications from trans-vaginal mesh and is currently accepting new cases on a contingency fee basis. If you or someone you love suffered revision surgery due to complications from trans-vaginal mesh, please call for a free consultation at 1-800-818-5329.

05/01/2014
Seithel Law, LLC

Trans-Vaginal Mesh Litigation Update

Endo International PLC (Endo) announced yesterday that it agreed to pay $830 Million to resolve legal claims from women who allege injuries by trans-vaginal mesh devices. Last year, Endo agreed to pay $54.5 Million to settle an undisclosed number of trans-vaginal mesh cases filed against them and their subsidiary American Medical Systems (AMS).

Endo and AMS along with other trans-vaginal mesh manufacturers are subject to lawsuits over mesh devices used to treat pelvic organ prolapse and stress-urinary incontinence. Women across the country allege that they suffered injuries requiring revision surgeries due to pain, erosion of the mesh, exposed mesh, incontinence symptoms and other complications.

As of February 20, 2014, approximately 22,000 lawsuits were filed against Endo and AMS in the mesh litigation according to the most recent annual filing with the Securities and Exchange Commission.

This agreement is expected to cover the substantial majority of the mesh litigation brought against Endo's subsidiary American Medical Systems. Neither Endo International PLC nor American Medical Systems admit any liability.

Seithel Law, LLC represents women who underwent revision surgery as a result of complications from trans-vaginal mesh and is currently accepting new cases on a contingency fee basis. If you or someone you love suffered revision surgery due to complications from trans-vaginal mesh, please call for a free consultation at 1-800-818-5329.

05/01/2014

Endo International PLC (Endo) announced yesterday that it agreed to pay $830 Million to resolve legal claims from women who allege injuries by trans-vaginal mesh devices. Last year, Endo agreed to pay $54.5 Million to settle an undisclosed number of trans-vaginal mesh cases filed against them and their subsidiary American Medical Systems (AMS).

Endo and AMS along with other trans-vaginal mesh manufacturers are subject to lawsuits over mesh devices used to treat pelvic organ prolapse and stress-urinary incontinence. Women across the country allege that they suffered injuries requiring revision surgeries due to pain, erosion of the mesh, exposed mesh, incontinence symptoms and other complications.

As of February 20, 2014, approximately 22,000 lawsuits were filed against Endo and AMS in the mesh litigation according to the most recent annual filing with the Securities and Exchange Commission.

This agreement is expected to cover the substantial majority of the mesh litigation brought against Endo's subsidiary American Medical Systems. Neither Endo International PLC nor American Medical Systems admit any liability.

Seithel Law, LLC represents women who underwent revision surgery as a result of complications from trans-vaginal mesh and is currently accepting new cases on a contingency fee basis. If you or someone you love suffered revision surgery due to complications from trans-vaginal mesh, please call for a free consultation at 1-800-818-5329.

Seithel Law, LLC's cover photo
04/14/2014

Seithel Law, LLC's cover photo

04/14/2014

76 Children who experienced birth defects after their mothers took Topamax during pregnancy settled lawsuits with the Johnson & Johnson and Janssen pharmaceutical companies last week.

These cases settled after several trials and jury verdicts in favor of the children and their families. Last month a jury awarded $3 Million in favor of a five year old whose lawyers claimed that Janssen did not update the Topamax label to reflect data showing that the drug resulted in an increased incidence of cleft lips and cleft palates in newborns when their mothers took Topamax during the first trimester of their pregnancies. A jury returned a $4 Million verdict against the company in a similar suit in October, 2013 and another family won a $10 Million verdict in December, 2013 against the makers of Topamax.

Topamax is an ant-epilepsy and migraine medication manufactured by Johnson & Johnson and its Janssen subsidiary.

In 2010, the United States Department of Justice reported that Ortho-McNeil Pharmaceutical LLC and Ortho-McNeil Janssen Pharmaceuticals Inc., both subsidiaries of Johnson & Johnson agreed to pay more than $81 Million to resolve criminal and civil liability arising from the illegal promotion of Topamax. The government alleged that the company promoted the sale of Topamax for off-label (unapproved) use through a practice known as the "Doctor-for-a-Day" program. Using this program, the company "hired outside doctors to join sales representatives on their visits to healthcare providers and to speak at meetings and dinners about prescribing Topamax for unapproved uses and doses."

Most pregnancies are unplanned and many women stop taking elective medications when they find out they are pregnant. Unfortunately by the time the moms stop taking the medications, babies may be exposed for weeks to medications that can cross the placenta barrier. During the first weeks of pregnancy critical fetal development can be affected by toxins that cross the placenta.

Often prior to pregnancy women are not aware of a medication's ability to cross the placenta, nor are they aware of adverse events reported to pharmaceutical companies bout birth defects that have occurred in children whose mothers took certain medications during pregnancy. Most mothers that we represent report that they would not have taken the medications at all or during a time period when they could become pregnant if they had known of the risk of birth defects.

Seithel Law, LLC represents children with birth defects whose mothers took Topamax, Depakote, Paxil, Zoloft or Effexor during the first trimester of pregnancy. We are currently accepting new cases. If you or a loved one you know has a child with birth defects and anti-depressants or Topamax could have been used in the first trimester of pregnancy, please contact Lynn Seithel directly at 843-557-1699 or 800-818-5329. Common birth defects our clients suffer from include but are not limited to: Cleft Lip, Cleft Palate, Atrial Septal Defect (ASD), Ventricular Septal Defect, (VSD), Transposition of the Greater Arteries (TGA), Tetralogy of Fallot, Spina Bifida, cranial defects and clubbed feet.

04/10/2014

Today The FDA announced a recall from Robert Abady Dog Food Co., LLC:

The Robert Abady Dog Food Co., LLC Recalls "Abady Highest Quality Maintenance & Growth Formula for Cats" Because of Possible Health Risk
04/09/2014 03:10 PM EDT

The Robert Abady Dog Food Co., LLC of Poughkeepsie, NY, is recalling its 2 lb, 5 lb & 15 lb boxes of "Abady Highest Quality Maintenance & Growth Formula for Cats" because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

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